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Recruiting NCT07380568

NCT07380568 Melatonin on Post Operative Pain After CS

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Clinical Trial Summary
NCT ID NCT07380568
Status Recruiting
Phase
Sponsor Benha University
Condition Pain Management
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2025-10-10
Primary Completion 2026-03-01

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 45 Years
Study Type INTERVENTIONAL
Interventions
Melatonin 5 mgMelatonin 10 mgPlacebo

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2025-10-10 with a primary completion date of 2026-03-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 Criteria

Inclusion Criteria: * \- Women aged 18-40 years. * Scheduled for elective cesarean section. * Ability to provide informed consent. Exclusion Criteria: * 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).

Frequently Asked Questions

Who can join the NCT07380568 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 45 Years, studying Pain Management. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07380568 currently recruiting?

Yes, NCT07380568 is actively recruiting participants. Visit ClinicalTrials.gov or contact Benha University to inquire about joining.

Where is the NCT07380568 trial being conducted?

This trial is being conducted at Banhā, Egypt.

Who is sponsoring the NCT07380568 clinical trial?

NCT07380568 is sponsored by Benha University. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology