A Randomized Controlled Crossover Study Comparing Sugammadex and Placebo

PHASE4CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

February 5, 2018

Primary Completion Date

December 30, 2019

Study Completion Date

April 30, 2020

Conditions
Posterior Cervical Decompression and Fusion
Interventions
DRUG

Sugammadex Injection [Bridion]

The study participants will receive 10 ml syringe containing Sugammadex (2mg/kg) in the first phase followed by Placebo 10 ml syringe containing of 0.9% of normal saline in the second phase.

DRUG

Placebo

The study participants will receive Placebo 10 ml syringe containing of 0.9% of normal saline in the first phase followed by 10 ml syringe containing Sugammadex (2mg/kg) in the second phase.

Trial Locations (1)

M5T 2S8

TWH/UHN, Toronto

All Listed Sponsors
collaborator

Merck Sharp & Dohme LLC

INDUSTRY

lead

University Health Network, Toronto

OTHER

NCT03087513 - A Randomized Controlled Crossover Study Comparing Sugammadex and Placebo | Biotech Hunter | Biotech Hunter