A clinical trial to study the effects of pre operative tablet melatonin in patients undergoing infra umbilical surgeries under spinal anaesthesia.
Not Applicable
Completed
- Conditions
- Health Condition 1: K460- Unspecified abdominal hernia withobstruction, without gangrene
- Registration Number
- CTRI/2018/08/015192
- Lead Sponsor
- Sagar Srinivas K
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 70
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
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain measured using VAS scoreTimepoint: Postoperative 24 hours
- Secondary Outcome Measures
Name Time Method Anxiety measured using HAM-A scaleTimepoint: Peri-operatively upto 24 hours after surgery