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A clinical trial to compare Sugammadex with Neostigmine for respiratory muscle strength recovery after neuromuscular blockade

Comparison Of Sugammadex With Neostigmine For Respiratory Muscle Strength Recovery After Neuromuscular Blockade - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073321
Enrollment
50
Registered
2024-09-04
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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: Patients will receive sugammadex 2 mg/kg at the end of Surgery Control Intervention1: Neostigmine: Patients will receive neostigmine 0.05mg/kg and 0.01mg/kg glycopyrrolate a

Sponsors

Dayanand Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for microlaryngeal surgeries. 2. Age - 18 to 65 years. 3. American Society of Anaesthesiologists (ASA) Physical Status Grade I-III 4. Either gender

Exclusion criteria

Exclusion criteria: 1. Pregnancy 2. BMI more than 35kg/m2 3. History of allergy to drugs used in study 4. Patient with severe liver (Child Pugh B or C class), renal (stage 4 kidney disease or higher), cardiac disease and/or rhythm disorder 5. Patient requiring postoperative reintubation, tracheostomy or mechanical ventilation. 6. Known or suspected neuromuscular disease 7. Patientââ?¬•s refusal to participate in the study

Design outcomes

Primary

MeasureTime frame
The change in diaphragm excursion from baseline (before induction of anaesthesia) to postextubation in both the groups.Timepoint: Post extubation

Secondary

MeasureTime frame
1 The change in diaphragm excursion from baseline to at 30 minutes in PACU in both the groups 2 The change in thickening fraction of internal oblique from baseline to post extubation & at 30 minutes in PACU in both the groups 3 The number of patients in whom diaphragm excursion & thickening fraction of internal oblique recovered to baseline level at post extubation & at 30 minutes in PACU in both the groupsTimepoint: Before Induction, Post extubation & at 30 min in PACU

Countries

India

Contacts

Public ContactDr Chaahat Sharma

Department of Anaesthesia

sharmachaahat012@gmail.com9815799085

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026