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

Efficacy of neostigmine in reversal of neuromuscular blockade in patients undergoing general anesthesia using cisatracurium - a randomized controlled clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067410
Enrollment
52
Registered
2024-05-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: Z00-Z99- Factors influencing health status and contact with health services

Interventions

Intervention1: 0.05 mg/kg Neostigmine diluted to 10ml with normal saline: Will be administered intravenously at the time of reversal. Control Intervention1: 10ml normal saline: Will be administered in

Sponsors

Dr Deepshikha Patangia
Lead Sponsor

Eligibility

Inclusion criteria

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

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).

Design outcomes

Primary

MeasureTime frame
To assess the time (in minutes) needed to achieve a TOF ratio of 0.9 after administering the study drug.Timepoint: 1. Preoperatively 2. Induction 3. Intubation 4. Extubation

Secondary

MeasureTime frame
1. To assess clinical parameters of postoperative recovery a. Sustained head lift(yes/no) b. Sustained hand grip(yes/no) c. Exhaled Tidal volume(in ml) 2. To assess length of Post Anesthesia Care Unit stay (in minutes) Timepoint: 1. Pre operatively 2. Induction 3. Intubation 4. Extubation

Countries

India

Contacts

Public ContactDr. Amrita Panda

Kalinga Institute of Medical Sciences

amrita.panda@kims.ac.in9439862335

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026