- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03825068
Erector Spinae Plane Block in Minimal Invasive Cardiac Surgery
March 9, 2020 updated by: Rasha Hamed, Assiut University
Studying the effect of erector spinae plane block in patients undergoing minimal invasive cardiac surgery.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: rasha hamed, lecturer
- Phone Number: 01000440773
- Email: rashaahmed11@yahoo.com
Study Locations
-
-
-
Assiut, Egypt, 71111
- Recruiting
- Assiut University
-
Contact:
- mohammed Ali Ahmed, MD
- Email: amira_salem2015@yahoo.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 50 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- elective valve replacement
Exclusion Criteria:
- chroic renal failure
- chronic liver failure
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: ESP block group
patients receive ESP Bock with local anaesthetics
|
20 ml of lacal anaesthetics will be placed below the erector spinae muscle under ultrasound guide
|
Placebo Comparator: control group
general anaestesia
|
patient receive general anaesthetic only
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
VAS
Time Frame: 48 hours
|
PAIN SCORES OF PATIENTS
|
48 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 15, 2018
Primary Completion (Anticipated)
November 30, 2020
Study Completion (Anticipated)
November 30, 2020
Study Registration Dates
First Submitted
January 30, 2019
First Submitted That Met QC Criteria
January 30, 2019
First Posted (Actual)
January 31, 2019
Study Record Updates
Last Update Posted (Actual)
March 10, 2020
Last Update Submitted That Met QC Criteria
March 9, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RRLL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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