Sponsor:
McGill University Health Centre/Research Institute of the McGill University Health Centre
Code:
NCT04256642
Conditions
Cesarean Section Complications
Eligibility Criteria
Sex: Female
Age: 18 - 45
Healthy Volunteers: Accepted
Interventions
Erector Spinae Plane Block
Intrathecal morphine
Brief summary:
Conditions
Cesarean Section Complications
Study ID
NCT04256642
Start date
Feb, 2020
Status verified date
Feb, 2020
Completion date
Jan, 2023
Anticipated
Primary completion date
Jan, 2022
Anticipated
Eligibility Criteria
Sex: Female
Age: 18 - 45
Healthy Volunteers: Accepted
Enrollment
160 participants
Anticipated
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary purpose
Treatment
Arms
active comparator: Intrathecal morphine
experimental: Erector Spinae Plane Block
Interventions
Erector Spinae Plane Block
Intrathecal morphine
Primary outcome measure
Central contacts
Locations
Royal Victoria Hospital
Recruiting
Montreal, Quebec, Canada
Contacts
Albert Moore, MD
moore_albert@hotmail.comSponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
Last update posted
Feb 5, 2020
Last verified
Feb, 2020
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by McGill University Health Centre/Research Institute of the McGill University Health Centre on 2020-02-05.