MedPath

Desflurane sparing effect of propofol and dexmedetomidine :A randomized study

Phase 1
Conditions
Health Condition 1: K807- Calculus of gallbladder and bile duct without cholecystitis
Registration Number
CTRI/2019/08/020485
Lead Sponsor
Sri Venkateswara Institute of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Elective laparoscopic surgeries

ASA I and II

Exclusion Criteria

Patients allergic or contraindications to study drugs

ASA III and above

Pregnant and lactating women

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Desflurane consumption <br/ ><br>Timepoint: Time to achieve Ramsay sedation score of 2, Time to reach modified Aldrete score of 9 post extubation and time taken for first analgesic request <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
PAIN ASSESMENT AND SEDATION SCORE ASSESMENTTimepoint: FROM POST EXTUBATION <br/ ><br>1]TIME TO FIRST ANALGESIC REQUEST[mins] <br/ ><br>2]TIME TAKEN TO REACH RAMSAY SEDATION SCORE OF 2[mins] <br/ ><br>3]TIME TAKEN TO REACH MODIFIED ALDRETE SCORE OF 9[mins]
© Copyright 2025. All Rights Reserved by MedPath