To determine the effectiveness of Demedetomidine given intraoperatively in decreasing analgesic requirement in postoperative period and enhancing recovery
Not Applicable
- Conditions
- Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system
- Registration Number
- CTRI/2024/04/065270
- Lead Sponsor
- Dr Shaila S Kamath
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Women aged 35-65 years
2)patients with ASA 1 & 2
3)patients undergoing elective gynecological surgeries under general anesthesia.
4)surgical time within 3 hours
Exclusion Criteria
1)Patients not willing to participate in the study
2)ASA 3 and above
3)Emergency gynecological surgeries
4) Patients with severe pulmonary, hepatic, cardiac, or renal disease
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) Postoperative analgesic requirement <br/ ><br>2) Recovery timeTimepoint: surgical time within 3hours
- Secondary Outcome Measures
Name Time Method 1) Hemodynamic variables <br/ ><br>2) Intraoperative blood lossTimepoint: Surgical time within 3 hours