Dexamethasone for Post-operative Pain After Cesarean Delivery Under Neuraxial Anesthesia.
NCT ID: NCT07257406
Last Updated: 2026-01-08
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
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COMPLETED
NA
87 participants
INTERVENTIONAL
2018-09-13
2025-10-01
Brief Summary
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Detailed Description
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In this randomised controlled trial, 100 patients are to be recruited and randomised to one of two groups. Both groups will receive standard treatment. In addition to standard treatment, the first group will receive dexamethasone 8 mg IV after umbilical cord clamping and the other group will receive a placebo.
The patients will be followed for 24 hours post-operatively. Their pain levels at rest and during movement will be recorded on an 11 point pain scale. The dose of hydromorphone used in the first 24 hours will be recorded. The patients are also asked to complete the QOR-40 questionnaire, which aims to assess the quality of their postoperative recovery. The primary outcome is the pain on an 11 point scale at the first rise 6 hours post-operatively.
The investigators hypothesize that dexamethasone will improve pain scores and diminish opioid use in the first 24 hours post-operatively.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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Dexamethasone
Dexamethasone (IV)
Dexamethasone 8 mg IV will be given 5 minutes after cord clamping in the interventional arm.
Placebo
Placebo
This arm will receive 2 ml of saline 5 min after cord clamping.
Interventions
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Dexamethasone (IV)
Dexamethasone 8 mg IV will be given 5 minutes after cord clamping in the interventional arm.
Placebo
This arm will receive 2 ml of saline 5 min after cord clamping.
Eligibility Criteria
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Inclusion Criteria
* Cesarean delivery
* Planned spinal or combined neuraxial anesthesia
* Presence of an investigator in the delivery room
* Pregnancy \> 34 weeks gestation
Exclusion Criteria
* Inability to understand French or English
* Allergy or hypersensitivity to dexamethasone
* Allergy to hydromorphone
* Allergy to NSAIDs
* Acute kidney injury or chronic kidney failure
* Preeclampsia
* Extremely urgent cesarean section
* Urgent cesarean section with non-reassuring fetal monitoring
* Known maternal heart disease
* High-grade placental abnormality
* Diabetes (pregnancy or pre-existing)
* Systemic infection, sepsis, fever
* Regular use of dexamethasone in the last year
* Weight greater than 120 kg and less than 70 kg
* Height less than 150 cm
* Chronic pain and/or chronic use of opioids
18 Years
FEMALE
No
Sponsors
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Université de Montréal
OTHER
Valerie Zaphiratos
OTHER
Responsible Party
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Valerie Zaphiratos
Associate Professor of Anesthesiology
Locations
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CHU Sainte-Justine
Montreal, Quebec, Canada
Countries
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References
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Mohtadi A, Nesioonpour S, Salari A, Akhondzadeh R, Masood Rad B, Aslani SM. The effect of single-dose administration of dexamethasone on postoperative pain in patients undergoing laparoscopic cholecystectomy. Anesth Pain Med. 2014 Aug 13;4(3):e17872. doi: 10.5812/aapm.17872. eCollection 2014 Aug.
Shahraki AD, Feizi A, Jabalameli M, Nouri S. The effect of intravenous Dexamethasone on post-cesarean section pain and vital signs: A double-blind randomized clinical trial. J Res Pharm Pract. 2013 Jul;2(3):99-104. doi: 10.4103/2279-042X.122370.
Cardoso MM, Leite AO, Santos EA, Gozzani JL, Mathias LA. Effect of dexamethasone on prevention of postoperative nausea, vomiting and pain after caesarean section: a randomised, placebo-controlled, double-blind trial. Eur J Anaesthesiol. 2013 Mar;30(3):102-5. doi: 10.1097/EJA.0b013e328356676b.
Other Identifiers
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2019-1840
Identifier Type: -
Identifier Source: org_study_id
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