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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04405336
Other study ID # tab block
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 28, 2020
Est. completion date April 1, 2021

Study information

Verified date May 2021
Source Aljazeera Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

cesarean section rate become increasing nowadays


Description:

indication of cesarean section are different from case to case and the use of pain controlling agents is very important to relieve post operative pain


Recruitment information / eligibility

Status Completed
Enrollment 140
Est. completion date April 1, 2021
Est. primary completion date March 15, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 42 Years
Eligibility Inclusion Criteria: - women coming for an elective CS Exclusion Criteria: - women who has a n emergency CS or complicated normal deivery needs urgent CS

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
tab block
injection of tab block to women who are doing cs
PCA
giving women PCA
women who will not receive tab block or PCA
no tab block or PCA will be given

Locations

Country Name City State
Egypt Aljazeera( Al Gazeera) hospital Giza

Sponsors (1)

Lead Sponsor Collaborator
Aljazeera Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of women who will feel less pain post CS the degree of pain that will be felt post CS 2 days
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