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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03825068
Other study ID # RRLL
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 15, 2018
Est. completion date November 30, 2020

Study information

Verified date March 2020
Source Assiut University
Contact rasha hamed, lecturer
Phone 01000440773
Email rashaahmed11@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Studying the effect of erector spinae plane block in patients undergoing minimal invasive cardiac surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date November 30, 2020
Est. primary completion date November 30, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- elective valve replacement

Exclusion Criteria:

- chroic renal failure

- chronic liver failure

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ESP Block
20 ml of lacal anaesthetics will be placed below the erector spinae muscle under ultrasound guide
Drug:
general anesthetic
patient receive general anaesthetic only

Locations

Country Name City State
Egypt Assiut university Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary VAS PAIN SCORES OF PATIENTS 48 hours
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