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Effectiveness of Neostigmine as reversal agent in patients undergoing general anesthesia with Cis-atracurium

Phase 3
Conditions
Health Condition 1: Z00-Z99- Factors influencing health status and contact with health services
Registration Number
CTRI/2024/05/067410
Lead Sponsor
Dr Deepshikha Patangia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients aged 20 to 60 years

2.American Society of Anesthesiology (ASA) physical status I and II

3.Scheduled for elective surgery under general anesthesia

4.Duration of surgery less than 3 hours.

Exclusion Criteria

1.Patients with a BMI = 25 kg/m2

2.Pregnant or lactating women

3.With significant hepatic or renal dysfunction

4.With respiratory pathologies like COPD or is a chronic smoker

5.Family history of malignant hyperthermia

6.Any known allergy to one of the drugs used in this protocol or on recent use of sedatives, anti-depressants

7.Inability to assess muscle strength or TOF count (neuromuscular disease).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the time (in minutes) needed to achieve a TOF ratio of 0.9 after administering the study drug.Timepoint: 1. Preoperatively <br/ ><br>2. Induction <br/ ><br>3. Intubation <br/ ><br>4. Extubation
Secondary Outcome Measures
NameTimeMethod
1. To assess clinical parameters of postoperative recovery <br/ ><br>a. Sustained head lift(yes/no) <br/ ><br>b. Sustained hand grip(yes/no) <br/ ><br>c. Exhaled Tidal volume(in ml) <br/ ><br>2. To assess length of Post Anesthesia Care Unit stay (in minutes) <br/ ><br>Timepoint: 1. Pre operatively <br/ ><br>2. Induction <br/ ><br>3. Intubation <br/ ><br>4. Extubation
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