Buscopan Versus Acetaminophen for Acute Abdominal Pain in Children
NCT ID: NCT02582307
Last Updated: 2019-05-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
PHASE3
236 participants
INTERVENTIONAL
2017-03-20
2019-02-22
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Ketorolac for Moderate to Severe Abdominal Pain in Children
NCT04528563
Intravenous Ketorolac Vs. Morphine In Children With Acute Abdominal Pain
NCT06160778
A Multi-Center Study of the Efficacy, Pharmacokinetics (PK) and Pharmacodynamics (PD) of IV Acetaminophen for the Treatment of Acute Pain in Pediatric Patients
NCT01635101
Comparison of the Effectiveness of Paracetamol With Ibuprofen or Paracetamol With Metamizole in Treating Pain in Acute Pancreatitis in Children
NCT07024199
Abdominal Pain Disorders Functional in Children: Impact of Hypno-analgesia on the Autonomic Balance
NCT02830698
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Hyoscine butylbromide
Hyoscine butylbromide 10mg oral single dose
Hyoscine butylbromide, Analgesics, Non-Narcotic
Oral single dose
Acetaminophen
Acetaminophen 15mg/kg oral single dose (maximum 1000mg)
Acetaminophen, Analgesics, Non-Narcotic
Oral single dose
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Acetaminophen, Analgesics, Non-Narcotic
Oral single dose
Hyoscine butylbromide, Analgesics, Non-Narcotic
Oral single dose
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
1. A chief complaint of colicky abdominal pain AND
2. Pain score of at least 4/10 on the Faces Pain Scale - Revised AND
3. A presumed non-surgical etiology
Exclusion Criteria
2. Concomitant use of other anticholinergic medication including but not limited to tricyclic antidepressants, antihistamines, benztropine mesylate
3. Signs and symptoms consistent with a bowel obstruction
4. Peritoneal signs
5. Suspected previous hypersensitivity reaction to either acetaminophen or HBB
6. Suspected appendicitis
7. History of abdominal trauma within 48 hours of presentation
8. Unstable vital signs
9. History of bowel obstruction
10. Myasthenia gravis
11. Fever (aural temperature \> 38.2 C)
12. Chronic liver disease
13. Persistent vomiting despite administration of oral anti-emetic
14. Symptoms and signs consistent with a urinary tract infection
15. Symptoms and signs consistent with a toxin ingestion
16. Symptoms and signs consistent with gynecological or gonadal pathology
17. Symptoms and signs consistent with vasoocclusive crisis in a patient with a hemoglobinopathy
8 Years
17 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Naveen Poonai, MD
Role: PRINCIPAL_INVESTIGATOR
Western University Health
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
London Health Sciences Centre
London, Ontario, Canada
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Poonai N, Kumar K, Coriolano K, Thompson G, Brahmbhatt S, Dzongowski E, Stevens H, Gupta P, Miller M, Elsie S, Ashok D, Joubert G, Lim R, Butter A, Ali S. Hyoscine butylbromide versus acetaminophen for nonspecific colicky abdominal pain in children: a randomized controlled trial. CMAJ. 2020 Nov 30;192(48):E1612-E1619. doi: 10.1503/cmaj.201055.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
107243
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.