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Assessment of three different doses of sugammadex for reversing the rocuronium induced neuromuscular blockade in laparoscopic cholecystectomy

Comparison of three different doses of sugammadex for reversal of rocuronium induced neuromuscular blockade in laparoscopic cholecystectomy:A Randomised Clinical trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107282
Enrollment
45
Registered
2026-04-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Sugammadex 1mg/kg: Study participants will be randomized into three groups.Intervention group will receive 1mg/kg of Inj. Sugammadex when the second Twitches to train of four stimulati

Sponsors

Rakshith C
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of either sex- male or female. 2.Patients of age group 18 to 60 years of Manipuri ethnicity undergoing elective laparoscopic cholecystectomy surgery under general anaesthesia. 3.Patients of American Society of Anaesthesiologists (ASA) physical status grade 1 or 2

Exclusion criteria

Exclusion criteria: 1.Patients not willing to participate. 2.Patients with known allergy to any of the study drugs. 3.Patients with known neuromuscular disease. 4.Patients with history of drug abuse (alcohol, sedative and analgesic 5.Patients with pre-existing conditions like respiratory, cardiovascular, hepatic or renal dysfunction etc 6.Patients with suspected malignant hyperthermia. 7.Pregnant and breast-feeding patients. 8.Patient who had joined in any studies in the past one month

Design outcomes

Primary

MeasureTime frame
The time taken from the start of administration of the study drugs (Sugammadex) at appearance of second twitch of train of four stimulation till recovery of normalised TOF ratio of 0.9 or more. Timepoint: Hemodynamic parameters such as blood pressure and heart rate at 5 minutes, thereafter for every 10 minutes intraoperatively and immediate postoperative period till one hour.

Secondary

MeasureTime frame
To compare the time taken to attain 5 seconds head lift from the start of administration of the study drug. Timepoint: Incidences of train of four normalised ratio of less than 0.9 during the first hour of postoperative period

Countries

India

Contacts

Public ContactTakhelmayum Hemjit Singh

Regional Institute of Medical Sciences Imphal

takhelhem@yahoo.com9436021445

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026