Clinical Trials Directory

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

TypeNameDescription
DRUGMelatonin 5 mgGroup I: (5 mg melatonin): Participants will receive 5 mg of oral melatonin 1 hours before the cesarean section.
DRUGMelatonin 10 mgGroup II: (10 mg melatonin): Participants will receive 10 mg of oral melatonin 1 hours before the cesarean section.
DRUGPlaceboGroup 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.