An act of comparing of three anesthetic drugs that is Dexmedetomidine- Ketamine- Propofol together compared with two drug group which is Ketamine-Propofol together for recovery quality
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/04/065195
- Lead Sponsor
- Baroda Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.patients posted for gynaecological procedure having procedure time less than 30 minutes
2.ASA I, II, III
3.age/ sex 18-65 years, female
4.BMI less than 30kg/ m2
5.patient belonging to mallamppati grading I- II on airway assessment
1.Inability or refusal to follow the study protocol
2.Patient with uncontrolled medical conditions like hypertension, diabetes mellitus, renal failure, active seizure, raised intracranial pressure etc.
3.Patient with sever cardiovascular or pulmonary pathology, sever renal or liver disorders.
4.Patient having neuro psychiatric disorders, H/o drug or alcohol abuse etc.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare post procedure recovery characteristics for: <br/ ><br>a)Recovery time (Time to achieve University of Michigan sedation scale 1 (UMSS 1)) <br/ ><br>b)Post procedure Emergence agitation: yes/no <br/ ><br>c)Over all patient satisfaction scoreTimepoint: At end of procedure
- Secondary Outcome Measures
Name Time Method 1.To monitor stability by monitoring systolic blood pressure, diastolic blood pressure, mean arterial pressure, pulse rate, peripheral oxygen saturation during procedure & maintain them within 20% of baseline value <br/ ><br>2.To record total requirement of incremental dose of ketamine-propofol during procedure <br/ ><br>3.Peri-procedure adverse events <br/ ><br>4.Post procedure discharge time will be observedTimepoint: From baseline till end of procedure