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efficacy of different doses of preoperative Melatonin on intraoprative blood loss and postoperative pain in patients undergoing cesarean section

Efficacy of different doses of preoperative melatonin on intraoperative blood loss and postoperative pain in patients undergoing cesarean section : clinical academic trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078540
Enrollment
120
Registered
2024-12-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: Melatonin drug: 3 mg melatonin by sublingual route to be given in women undergoing section 30 min before spinal only single dose Intervention2: melatonin 6 mg: melatonin 6 mg sublingual

Sponsors

Trupti kamble
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Single cephalic term gestation pregnant women

Exclusion criteria

Exclusion criteria: Allergy to melatonin Twin gestation

Design outcomes

Primary

MeasureTime frame
decrease in blood loss analgesic effectTimepoint: 24 hours—

Secondary

MeasureTime frame
analgesic effect & sleep qualityTimepoint: analgesic effect 48 hrs after surgery analgesic effect 72 hours after surgery—

Countries

India

Contacts

Public ContactDr.sairem mangolnabi Chanu

AIIMS Mangalgiri Andhrapradesh

dr.mangol123@gmail.com8794713545

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026