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A study comparing recovery features of patients undergoing general anaesthesia with rocuronium as muscle relaxant and recieving sugammadex or neostigmine and glycopyrollate for reversal.

A study comparing recovery characteristics of patients recieving either Sugammadex or Neostigmine and Glycopyrollate, for reversal of rocuronium induced Neuromuscular block - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065600
Enrollment
109
Registered
2024-04-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: K402- Bilateral inguinal hernia, withoutobstruction or gangrene Health Condition 2: K800- Calculus of gallbladder with acutecholecystitis Health Condition 3: N920- Excessive and frequent menstruation with regular cycle

Interventions

Intervention1: Sugammadex: 2mg/kg given at TOF count of 2. Given only once at the time of extubation. Control Intervention1: Neostigmine and Glycopyrollate: Neostigmine 2.5 mg and glycopyrollate 0.4 m

Sponsors

Manipal Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists grades 1, 2, and 3 patients aged 18–60 years, coming for elective laparoscopic surgeries (lasting one to three hours) will be recruited for the study.

Exclusion criteria

Exclusion criteria: 1. Patients with cardiorespiratory abnormalities (New York Heart Association heart failure grades 3 and 4. 2. Known allergy to Rocuronium. 3. Renal insufficiency (eGFR 4. Liver dysfunction (liver enzymes—serum glutamic oxaloacetic transaminase/ serum glutamic pyruvic transaminase values elevated by more than 50% of normal). • Underlying neuromuscular disease or the use of drugs known to interfere with neuromuscular transmission. • Intraoperative hypothermia (core temperature less than 35°C). • Known Emphysema. • Unwillingless to perform PFT.

Design outcomes

Primary

MeasureTime frame
Time taken for complete reversal of neuromuscular blockTimepoint: Reversal given at TOF count of 2 and time taken to reach TOF ratio 0.9. It is checked at the end of each case at the time of extubation.

Secondary

MeasureTime frame
To compare post operative respiratory function in terms of PFTTimepoint: PFT to be done in post anaesthesia care unit 20 minute after extubation

Countries

India

Contacts

Public ContactSameer Akthar B

Manipal Hospital

drhsmurthy@gmail.com8111053116

Outcome results

None listed

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