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Comparison between sugammadex and neostigmine for reversal of blockade in neurosurgery patients

A Comparative Study of Sugammadex versus Neostigmine for Reversal of Vecuronium-Induced Neuromuscular Blockade Following Intracranial Tumor Resection Surgery In Adults - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/068057
Enrollment
50
Registered
2024-05-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: G969- Disorder of central nervous system, unspecified Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Sugammadex: Group S will be administered Sugammadex . Dose -2mg/kg frequency - once route of adminstration -Intravenous total duration of such intervention - 24hours Control Intervent

Sponsors

Jawaharlal Nehru Medical CollegeDatta Meghe Institute of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a. Inclusion Criteria: 1. Consenting adults, undergoing elective intracranial tumor surgery under general anaesthesia with Vecuronium-induced neuromuscular blockade. 2.Adult patient above age of 18yrs -65yrs 3.No comorbidity 4.GCS –15/15

Exclusion criteria

Exclusion criteria: 1.Patients with contraindications to Sugammadex or Neostigmine 2.Pre-existing neuromuscular disorders 3. Those requiring prolonged postoperative ventilation. 4.Malignant hyperthermia

Design outcomes

Primary

MeasureTime frame
Time taken for the reversal of neuromuscular blockade Timepoint: 1 hour

Secondary

MeasureTime frame
2. Incidence of residual neuromuscular blockade post-reversal. 3. Recovery of neuromuscular function assessed via train-of-four ratio or similar monitoring methods. 4. Safety outcomes: Respiratory events, hemodynamic instability, and occurrence of cholinergic side effects. 5. Emergence from anesthesia and time to extubation. Timepoint: 1 hour

Countries

India

Contacts

Public ContactAishwarya Nayak

Jawaharlal Nehru Medical College,Datta Meghe Institute of Higher Education and Research

dr.roshannisal@gmail.com8249892501

Outcome results

None listed

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