Trials / Recruiting
RecruitingNCT07380568
Melatonin on Post Operative Pain After CS
The Effect of Preoperative Oral Melatonin on Postoperative Pain Control After Cesarean Section: A Dose Comparison Study
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Benha University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this clinical trial is to learn if melatonin will decrease pain after C.S. The main questions it aims to answer are: Does melatonin lower the number of times participants need to use a rescue analgesia? What medical problems do participants have when taking melatonin? Researchers will compare different doses of melatonin to see the ideal dose to decrease pain after C.S. Participants will: Take melatonin 30 min before C.S and will be observed for 24 hours for pain and consumption of other analgesia
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Melatonin 5 mg | Group I: (5 mg melatonin): Participants will receive 5 mg of oral melatonin 1 hours before the cesarean section. |
| DRUG | Melatonin 10 mg | Group II: (10 mg melatonin): Participants will receive 10 mg of oral melatonin 1 hours before the cesarean section. |
| DRUG | Placebo | Group III: (Placebo): Participants will receive an identical placebo tablet 1 hours before the cesarean section. |
Timeline
- Start date
- 2025-10-10
- Primary completion
- 2026-03-01
- Completion
- 2026-04-01
- First posted
- 2026-02-02
- Last updated
- 2026-02-02
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT07380568. Inclusion in this directory is not an endorsement.