The Ondansetron Premedication Trial in Juvenile Idiopathic Arthritis
NCT ID: NCT04169828
Last Updated: 2025-06-29
Study Results
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Basic Information
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COMPLETED
NA
52 participants
INTERVENTIONAL
2019-08-02
2025-01-17
Brief Summary
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Detailed Description
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To evaluate if routine pre-medication with the anti-emetic ondansetron reduces methotrexate intolerance and increases the proportion of children with JIA able to continue taking methotrexate, resulting in a better quality of life and more cost-effective medication use.
2. Hypothesis:
Prophylactic prescription of ondansetron with methotrexate will increase the proportion of children that remain on methotrexate and intolerance free one year after starting methotrexate, relative to prescription of ondansetron after intolerance symptoms develop.
3. Justification:
Methotrexate intolerance is thought to be largely the result of Pavlovian conditioning secondary to previous exposure and symptoms can be triggered by associated stimuli, such as a yellow liquid similar in color to methotrexate or the smell of alcohol cleansing swabs. This intolerance leads to poor adherence to optimal dosing or to stopping the medication altogether. Children who cannot adhere to optimal dosing or stop methotrexate may require expensive biologic medications to control their JIA. Methotrexate intolerance often leads to use of anti-emetic medications which, unfortunately, rarely reverse conditioned responses. In oncology anti-emetics are used prophylactically as premedication in all subjects receiving chemotherapy to prevent the establishment of conditioned intolerance.
By conducting a registry-based pragmatic adaptive superiority randomized clinical trial the investigators will include most subjects in whom the treatment may be used under the usual conditions of practice to demonstrate effectiveness under real word circumstances. Patients enrolled in a pragmatic trial are more representative because eligibility criteria are less strict. More so, a registry-based pragmatic RCT can also be much cheaper than a traditional RCT.
4. Objectives:
The investigators will assign patients starting low-dose methotrexate for JIA 1:1 online using the CAPRI Registry and block randomization by Canadian region and patient weight to one of two groups:
Intervention: Routine premedication with oral ondansetron (2, 4 or 8 mg for patient weights \<15Kg, 15-30Kg, \>30 Kg; 3 doses a week).
Control: Oral ondansetron at the same dosing, prescribed only to those patients who develop methotrexate-induced nausea/vomiting during usual care.
The investigators will compare:
1. The proportions of patients remaining on methotrexate with no intolerance between the two groups one year after starting methotrexate (primary objective).
2. Safety and tolerability
3. The cumulative incidence of:
1. methotrexate intolerance
2. attainment of inactive disease
3. biologic medication initiation
4. The mean quality of life scores and methotrexate intolerance severity scores between the two groups 4-8 months after starting methotrexate.
The investigators will also collect information on impacts on quality of life and medication utilization that will enable a future cost-effectiveness analysis.
5. Research Design:
The investigators will conduct a CAPRI JIA Registry-based pragmatic adaptive superiority RCT as per the following methods.
Registry-based: The trial will use infrastructure already in place for the CAPRI JIA Registry.
Pragmatic: Broad inclusion criteria and simple outcome assessments compatible with usual care.
Adaptive: This is a Planned Sample-Size Re-Estimation Adaptive Trial as described by Bhatt \& Metha \[34\].
Superiority: Designed to test superiority (as opposed to non-inferiority) of ondansetron premedication.
RCT: Treatments assigned by block randomization and analyses adjusted for post-randomization imbalances
6. Statistical Analysis:
The primary outcome statistic is the ratio of two proportions (relative risk, RR), the proportion of children remaining on methotrexate with no intolerance in the intervention group divided by the same in the control group. This choice allows flexibility for the frequency of follow-up visits to be set-up as per clinical need, obviating the need for study-specific visits, increasing feasibility and decreasing costs. It is also not impacted by the times at which methotrexate intolerance or discontinuation occur which leads to simplicity in interpretation and analysis.
The sample size calculation is based on expressing the RR in the log scale and using established formulas for standard errors. With p\<0.05, power of 90% and expected methotrexate continuation with no intolerance of 50% in the control group and 75% in the intervention group the result is 79 evaluable subjects per group. The investigators will aim to recruit 176 subjects total to allow for up to a 10% dropout rate, although they expect a dropout rate of \<5% based on previous CAPRI studies.
A preliminary analysis after recruitment of 90 subjects will consist of a two-sided confidence interval (CI) for the RR of continuing on methotrexate with no intolerance, where the confidence level is adjusted for information accrual as per Schoenfeld.
The Data and Safety Committee will assess preliminary results according to the following guidance:
If the CI is entirely below a relative risk of 1.2, the study will be stopped for futility.
If the CI is entirely above a relative risk of 1.2, the study will be stopped and superiority will be claimed.
If the CI includes a relative risk of 1.2, the trial will continue until the re-calculated full target sample is attained.
The RR of 1.2 has been selected on clinical grounds. In a prospective study of 142 children with JIA starting methotrexate followed for one year, Van Dijkhuizen et al reported that 59 patients developed intolerance and 11 discontinued methotrexate for other reasons, for a total of 72 (50.7%) remaining on methotrexate with no intolerance. An increase in this proportion to \<60% is deemed too small to justify the additional costs and risks of adding prophylactic ondansetron.
The final analysis will be an intention to treat analysis conducted after the final sample size is achieved or at the time the study is stopped. All subjects enrolled in the study at that time will complete a one-year follow-up and will be included in the final analysis. Logistic regression models will be used to adjust effect estimates for post-randomization imbalances in the two groups (intervention, control). A secondary per-protocol analysis will be conducted on those subjects who received the assigned intervention for at least 3 months.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Ondansetron premedication
Methotrexate and folic/folinic acid as prescribed by physician. Ondansetron: 2 mg if \<15Kg, 4 mg if 15-30Kg, 8 mg if \>30Kg to be taken by mouth one hour before each weekly methotrexate dose, followed by two additional doses every 6-8 hours if awake. To be started from the very first dose of methotrexate.
Methotrexate
Children in both the intervention and control group will receive Methotrexate dosed as prescribed by the attending rheumatologist
Ondansetron
Children in the intervention group will be prescribed premedication with oral ondansetron.
Children in the control group will be prescribed ondansetron ONLY if the child reports nausea/vomiting during regular treatment care with Methotrexate
Folic/folinic acid
Children in both intervention and control group will receive folic acid or folinic acid dosed as prescribed by the attending rheumatologist.
Ondansetron as needed
Methotrexate and folic/folinic acid as prescribed by physician. ONLY children who report nausea/vomiting during regular care will be prescribed ondansetron at the same dose as in experimental group (2 mg if \<15Kg, 4 mg if 15-30Kg, 8 mg if \>30Kg to be taken by mouth one hour before each weekly methotrexate dose, followed by two additional doses every 6-8 hours if awake), as per the attending rheumatologist's discretion
Methotrexate
Children in both the intervention and control group will receive Methotrexate dosed as prescribed by the attending rheumatologist
Ondansetron
Children in the intervention group will be prescribed premedication with oral ondansetron.
Children in the control group will be prescribed ondansetron ONLY if the child reports nausea/vomiting during regular treatment care with Methotrexate
Folic/folinic acid
Children in both intervention and control group will receive folic acid or folinic acid dosed as prescribed by the attending rheumatologist.
Interventions
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Methotrexate
Children in both the intervention and control group will receive Methotrexate dosed as prescribed by the attending rheumatologist
Ondansetron
Children in the intervention group will be prescribed premedication with oral ondansetron.
Children in the control group will be prescribed ondansetron ONLY if the child reports nausea/vomiting during regular treatment care with Methotrexate
Folic/folinic acid
Children in both intervention and control group will receive folic acid or folinic acid dosed as prescribed by the attending rheumatologist.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Diagnosis of JIA as per ILAR criteria \[1\], irrespective of JIA category
3. Followed at a CAPRI centre in Canada
4. Starting methotrexate to control JIA manifestations (arthritis, uveitis, psoriasis). (Female subjects of child bearing potential who are taking methotrexate for JIA cannot be pregnant, breastfeeding, or planning a pregnancy while on the drug and females of childbearing potential who are sexually active must use highly effective medically acceptable contraception. Subjects who stop methotrexate during the study will also discontinue ondansetron.)
5. Informed written consent to participate
6. Participating in the CAPRI JIA Registry
Exclusion Criteria
2. Known hypersensitivity to ondansetron or any components of its formulations
3. Known hypersensitivity to other 5-HT3 antagonists
4. Known congenital Long-QT syndrome
5. Patients taking other medicinal products that lead to either QT prolongation or electrolyte abnormalities
6. Because the serotonin syndrome may occur when ondansetron is combined with other agents that may affect the serotonergic neurotransmitter system, patients receiving any of the serotonergic and/or neuroleptic drugs listed below will be excluded:
• Triptans, SSRIs, SNRIs, lithium, sibutramine, fentanyl and its analogues, dextromethorphan, tramadol, tapendalol, meperidine, methadone, pentazocine or St. John's Wort (Hypericum perforatum), MAOIs, linezolid, methylene blue.
7. Patients who are pregnant or breastfeeding, or are sexually active and unwilling to practice an acceptable method of birth control.
8. Family unable to complete questionnaires in English or French
4 Years
16 Years
ALL
No
Sponsors
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The Arthritis Society, Canada
OTHER
University of Calgary
OTHER
The Hospital for Sick Children
OTHER
McGill University Health Centre/Research Institute of the McGill University Health Centre
OTHER
London Health Sciences Centre
OTHER
University of Manitoba
OTHER
Alberta Children's Hospital
OTHER
McMaster University
OTHER
McMaster Children's Hospital
OTHER
Université de Montréal
OTHER
University of British Columbia
OTHER
Responsible Party
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Jaime Guzman
Principle Investigator
Principal Investigators
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Jaime Guzman, MD, FRCPC
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Locations
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University of Calgary / Alberta Children's Hospital
Calgary, Alberta, Canada
University of Alberta
Edmonton, Alberta, Canada
BC Children's Hospital
Vancouver, British Columbia, Canada
University of Manitoba/Children's hospital research institute
Winnipeg, Manitoba, Canada
McMaster University/McMaster Children's Hospital
Hamilton, Ontario, Canada
London Health Sciences Centre
London, Ontario, Canada
Hospital for Sick Children
Toronto, Ontario, Canada
McGill University Health Centre
Montreal, Quebec, Canada
Université de Montréal
Montreal, Quebec, Canada
CHU de Quebec - Universite Laval
Québec, Quebec, Canada
Royal University Hospital
Saskatoon, Saskatchewan, Canada
Countries
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References
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Guzman J, Oen K, Tucker LB, Huber AM, Shiff N, Boire G, Scuccimarri R, Berard R, Tse SM, Morishita K, Stringer E, Johnson N, Levy DM, Duffy KW, Cabral DA, Rosenberg AM, Larche M, Dancey P, Petty RE, Laxer RM, Silverman E, Miettunen P, Chetaille AL, Haddad E, Houghton K, Spiegel L, Turvey SE, Schmeling H, Lang B, Ellsworth J, Ramsey S, Bruns A, Campillo S, Benseler S, Chedeville G, Schneider R, Yeung R, Duffy CM; ReACCh-Out investigators. The outcomes of juvenile idiopathic arthritis in children managed with contemporary treatments: results from the ReACCh-Out cohort. Ann Rheum Dis. 2015 Oct;74(10):1854-60. doi: 10.1136/annrheumdis-2014-205372. Epub 2014 May 19.
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van Dijkhuizen EH, Bulatovic Calasan M, Pluijm SM, de Rotte MC, Vastert SJ, Kamphuis S, de Jonge R, Wulffraat NM. Prediction of methotrexate intolerance in juvenile idiopathic arthritis: a prospective, observational cohort study. Pediatr Rheumatol Online J. 2015 Feb 18;13:5. doi: 10.1186/s12969-015-0002-3. eCollection 2015.
Bechard MA, Lemieux JR, Roth J, Watanabe Duffy K, Duffy CM, Aglipay MO, Jurencak R. Procedural pain and patient-reported side effects with weekly injections of subcutaneous methotrexate in children with rheumatic disorders. Pediatr Rheumatol Online J. 2014 Dec 19;12:54. doi: 10.1186/1546-0096-12-54. eCollection 2014.
Klotsche J, Minden K, Niewerth M, Horneff G. Time spent in inactive disease before MTX withdrawal is relevant with regard to the flare risk in patients with JIA. Ann Rheum Dis. 2018 Jul;77(7):996-1002. doi: 10.1136/annrheumdis-2017-211968. Epub 2018 Feb 16.
Scheuern A, Tyrrell PN, Haas JP, Hugle B. Countermeasures against methotrexate intolerance in juvenile idiopathic arthritis instituted by parents show no effect. Rheumatology (Oxford). 2017 Jun 1;56(6):901-906. doi: 10.1093/rheumatology/kew507.
Schoemaker CG, van Dijkhuizen EHP, Vastert SJ. Contradictory and weak evidence on the effectiveness of anti-emetics for MTX-intolerance in JIA-patients. Pediatr Rheumatol Online J. 2018 Feb 15;16(1):13. doi: 10.1186/s12969-018-0229-x. No abstract available.
Phillips RS, Friend AJ, Gibson F, Houghton E, Gopaul S, Craig JV, Pizer B. Antiemetic medication for prevention and treatment of chemotherapy-induced nausea and vomiting in childhood. Cochrane Database Syst Rev. 2016 Feb 2;2(2):CD007786. doi: 10.1002/14651858.CD007786.pub3.
Cubeddu LX, Hoffmann IS, Fuenmayor NT, Finn AL. Efficacy of ondansetron (GR 38032F) and the role of serotonin in cisplatin-induced nausea and vomiting. N Engl J Med. 1990 Mar 22;322(12):810-6. doi: 10.1056/NEJM199003223221204.
De Mulder PH, Seynaeve C, Vermorken JB, van Liessum PA, Mols-Jevdevic S, Allman EL, Beranek P, Verweij J. Ondansetron compared with high-dose metoclopramide in prophylaxis of acute and delayed cisplatin-induced nausea and vomiting. A multicenter, randomized, double-blind, crossover study. Ann Intern Med. 1990 Dec 1;113(11):834-40. doi: 10.7326/0003-4819-113-11-834.
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Blanco R, Gonzalez-Gay MA, Garcia-Porrua C, Ibanez D, Garcia-Pais MJ, Sanchez-Andrade A, Vazquez-Caruncho M. Ondansetron prevents refractory and severe methotrexate-induced nausea in rheumatoid arthritis. Br J Rheumatol. 1998 May;37(5):590-2. doi: 10.1093/rheumatology/37.5.590. No abstract available.
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Wallace CA, Giannini EH, Huang B, Itert L, Ruperto N; Childhood Arthritis Rheumatology Research Alliance; Pediatric Rheumatology Collaborative Study Group; Paediatric Rheumatology International Trials Organisation. American College of Rheumatology provisional criteria for defining clinical inactive disease in select categories of juvenile idiopathic arthritis. Arthritis Care Res (Hoboken). 2011 Jul;63(7):929-36. doi: 10.1002/acr.20497.
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Provided Documents
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Document Type: Statistical Analysis Plan
Related Links
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Health Canada prescribing information for methotrexate.
Hopper C, Khan S, Mancini J, Rennick J. Perceptions of Methotrexate Intolerance in School-aged Children With Juvenile Idiopathic Arthritis \[abstract\].Arthritis Rheumatol. 2017; 69 (suppl 4).
Da Silva C, Farias A, Sinicato N, Veloso R, Marini R, Appenseller S. Reasons for stopping methotrexate treatment in patients with juvenile idiopathic arthritisPediatric Rheumatology 2014, 12(Suppl 1):P199 (abstract)
Health Canada prescribing information for ondansetron
Ontario Drug Benefit Formulary
Other Identifiers
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H18-03176
Identifier Type: -
Identifier Source: org_study_id
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