Comparison of sedative medication to non-sedative medication for pain relief during and after laproscopic surgery
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2020/08/027401
- Lead Sponsor
- Pramukhswami medical College Shree Krishna Hospital Bhaikaka University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Adult patients aged 18 to 60 years who can give informed consent and posted for laproscopic surgeries who belong to American society of anaesthesiologist physical status grade 1 to 3 are included for the study.
ASA grade 4 and 5 patients, patients with hepatic,cardiac renal insufficiency, Body mass index >40,pregnant and breast feed patients,patients with conduction defect and basal heart rate <50 beats per minute and patients with psychiatric illness, intracranial pathology and who are not willing to give consent are excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method