RecruitingNot ApplicableNCT07380568

Melatonin on Post Operative Pain After CS

The Effect of Preoperative Oral Melatonin on Postoperative Pain Control After Cesarean Section: A Dose Comparison Study


Sponsor

Benha University

Enrollment

60 participants

Start Date

Oct 10, 2025

Study Type

INTERVENTIONAL

Conditions

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


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 45 Years

Inclusion Criteria3

  • \- Women aged 18-40 years.
  • Scheduled for elective cesarean section.
  • Ability to provide informed consent.

Exclusion Criteria7

  • Known hypersensitivity to melatonin or opioids
  • Chronic use of analgesics, sedatives, or antidepressants.
  • History of sleep disorders or psychiatric illness.
  • Complicated pregnancies (e.g., preeclampsia, gestational diabetes).
  • Body mass index (BMI) \> 35 kg/m².
  • Emergency cesarean sections.
  • Severe systemic diseases (e.g., liver or kidney dysfunction).

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Interventions

DRUGMelatonin 5 mg

Group I: (5 mg melatonin): Participants will receive 5 mg of oral melatonin 1 hours before the cesarean section.

DRUGMelatonin 10 mg

Group II: (10 mg melatonin): Participants will receive 10 mg of oral melatonin 1 hours before the cesarean section.

DRUGPlacebo

Group III: (Placebo): Participants will receive an identical placebo tablet 1 hours before the cesarean section.


Locations(1)

Benha University Hospital

Banhā, Egypt

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NCT07380568


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