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A clinical trial to study the effects of pre operative tablet melatonin in patients undergoing infra umbilical surgeries under spinal anaesthesia.

Efficacy of pre-operative oral melatonin on post-operative pain in patients undergoing infra-umbilical surgeries under subarachnoid block- a double blind randomised control study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015192
Enrollment
70
Registered
2018-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K460- Unspecified abdominal hernia withobstruction, without gangrene

Interventions

None listed

Sponsors

Sagar Srinivas K
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who have given written informed consent. Patients with ASA grade I & II. Patients scheduled for elective infra-umbilical surgeries under subarachnoid block.

Exclusion criteria

Exclusion criteria: Patients refusing to participate in the study. Patients with history of psychiatric disorders on antipsychotic drugs. Patients with history of sleep disorders. Patients on anticoagulants. Patients with hypertension, type2 DM, IHD. Pregnant women. Contraindication to spinal anaesthesia.

Design outcomes

Primary

MeasureTime frame
Postoperative pain measured using VAS scoreTimepoint: Postoperative 24 hours—

Secondary

MeasureTime frame
Anxiety measured using HAM-A scaleTimepoint: Peri-operatively upto 24 hours after surgery—

Countries

India

Contacts

Public ContactSagar Srinivas K

Bangalore Medical College and Research Institute

nethra.surhonne@gmail.com9448171403

Outcome results

None listed

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