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NCT05202899 Clinical Trial

Effect of Sugammadex for Reversal of Rocuronium-induced Neuromuscular Block on Perioperative Management of Awake Craniotomy

Brain Tumors Clinical Trial

Official title:
Effect of Sugammadex for Reversal of Rocuronium-induced Neuromuscular Block on Perioperative Management of Awake Craniotomy

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05202899
Other study ID # Awake Craniotomy
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date September 1, 2020
Est. completion date May 31, 2022

Study information
Verified date March 2022
Source Guangzhou General Hospital of Guangzhou Military Command
Contact bo xu, DR
Phone 88653387
Email xubo333@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Effect of sugammadex for reversal of rocuronium-induced neuromuscular block on Perioperative Management of awake Craniotomy

Recruitment information / eligibility
Status Recruiting
Enrollment 40
Est. completion date May 31, 2022
Est. primary completion date February 28, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Age: 18-45 years old body mass index (BMI)= 18.5-23.9 kg/m2, ASA grade I ~II. Exclusion Criteria: - Suffering from a mental illness or preoperative communication disorder, patients with claustrophobia, breathing, circulation, neuromuscular system and kidney, and other important viscera function disorder, pregnant or lactating women, a history of malignant hyperthermia, the history of drug allergy in the process of general anesthesia and recent may not used to the interaction between rocuronium, vecuronium bromide reacts drugs (such as aminoglycoside antibiotics, Anticonvulsant, magnesium).

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• sugammadex
The use of sugammadex

Locations
Country Name City State
China Guangzhou Military Region General Hospital, Department of Anesthesiology Guangzhou Guangdong

Sponsors (1)
Lead Sponsor Collaborator
Guangzhou General Hospital of Guangzhou Military Command

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary awake time The time between asleep and awake 10-30 minutes
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