NCT01662219View on ClinicalTrials.gov

Effect of Superficial Cervical Plexus Block on the Postoperative Quality of Recovery

NACompletedINTERVENTIONAL
Enrollment

46

Participants

Timeline

Start Date

August 31, 2012

Primary Completion Date

June 30, 2014

Study Completion Date

June 30, 2014

Conditions
Cervical Disc Prolapse
Interventions
OTHER

Superficial cervical plexus block for experimental group

15 ml of 0.25% Bupivacaine will be given for superficial cervical plexus block

Trial Locations (1)

M5T2S8

Toronto Western Hospital,UHN., Toronto

All Listed Sponsors
lead

University Health Network, Toronto

OTHER

NCT01662219 - Effect of Superficial Cervical Plexus Block on the Postoperative Quality of Recovery | Biotech Hunter | Biotech Hunter