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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

Phase 4
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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
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
NameTimeMethod
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
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