ClinicalTrials.Veeva

Menu

The Dose of Sugammadex for Rapid Reversal of Profound Neuromuscular Block in Young and Elderly Patients

Yonsei University logo

Yonsei University

Status

Completed

Conditions

Anesthesia Recovery Period, Neuromuscular Blockade

Treatments

Drug: Sugammadex

Study type

Interventional

Funder types

Other

Identifiers

NCT01890057
4-2013-0280

Details and patient eligibility

About

To find out the dose of sugammadex for recovery of the TOF ratio to 0.9 within 2 minutes from profound rocuronium-induced neuromuscular block in young and elderly adult patients.

Full description

A previous study reported that elderly patients required a longer time to recover from rocuronium induced neuromuscular block compared to younger patients. Therefore, the aim of this study is to find out the dose of sugammadex for rapid recovery from profound neuromuscular block in young and elderly adult patients.

Enrollment

44 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 20-40 years or ≥70 years ASA class I-II patients who received surgery less than 2 hours.

Exclusion criteria

  • anticipated difficult intubation
  • neuromuscular, hepatic or renal disorders
  • drug allergy
  • body mass index >30 kg/m2 or body mass index <18 kg/m2
  • emergency surgery

Trial design

44 participants in 2 patient groups

Young adults
Experimental group
Description:
To find out the the dose of sugammadex for recovery of the TOF ratio to 0.9 within 2 minutes from profound neuromuscular block : Dixon's up-and-down method
Treatment:
Drug: Sugammadex
Elderly adults
Experimental group
Description:
To find out the the dose of sugammadex for recovery of the TOF ratio to 0.9 within 2 minutes from profound neuromuscular block : Dixon's up-and-down method
Treatment:
Drug: Sugammadex

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems