Skip to content

Comparison of two drugs used for reversal of muscle blockade in older adult patients undergoing bronchoscopy

Comparison of recovery characteristics of sugammadex versus neostigmine in older adult patients undergoing bronchoscopy: A randomised controlled trial - nil

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107736
Enrollment
50
Registered
2026-04-07
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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: Group A will receive sugammadex as reversal agent: Group A participants will receive 2mg/kg of Sugammadex IV when spontaneous recovery had reached a second twitch after TOF, or 4 mg/Kg

Sponsors

All India institute of medical sciences- Rishikesh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age: more than or equal to 50 years 2.ASA class I or II or III 2. All patients undergoing diagnostic or therapeutic bronchoscopy 3.Patients giving consent for procedure.

Exclusion criteria

Exclusion criteria: 1.Patient already underwent any thoracic surgery in the past. 2.Patient with ventilated support 3.severe cardiac diseases (EF less than 30%) 4.History of allergy to any reversal drugs.

Design outcomes

Primary

MeasureTime frame
extubation time in the older adult patient under going bronchoscopyTimepoint: At the time of extubation of trachea

Secondary

MeasureTime frame
1.To compare intraoperative and post operative vitals (heart rate, Spo2, BP) related to use of Sugammadex vs Neostigmine 2.to compare the post operative residual paralysis/pulmonary function after reversal from neuromuscular blockade by Sugammadex vs Neostigmine based on breath holding time after 60 minutes of extubation . 3.Compare any complications associated with use of Sugammadex vs Neostigmine like hypotension, bronchospasm, apnea, pneumonia, atelectasis etc. Timepoint: During intraoperative period and 1 hour of post extubation in PACU

Countries

India

Contacts

Public ContactDr Mridul Dhar

All India institute of medical sciences- Rishikesh

mriduldhar87@gmail.com9717778374

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026