- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04405336
Tab Block and Patient Controlled Analgesia in CS
May 21, 2021 updated by: Aljazeera Hospital
Effect of Tab Block and Patient Controlled Analgesia in Cesarean Section
cesarean section rate become increasing nowadays
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed 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
Study Type
Interventional
Enrollment (Actual)
140
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 Locations
-
-
-
Giza, Egypt
- Aljazeera( Al Gazeera) hospital
-
-
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
18 years to 42 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
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 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: SUPPORTIVE_CARE
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: giving tab block
giving patients tab block
|
injection of tab block to women who are doing cs
no tab block or PCA will be given
|
|
ACTIVE_COMPARATOR: giving PCA
Giving PCA to patients
|
no tab block or PCA will be given
giving women PCA
|
|
NO_INTERVENTION: Patients who will not receive PCA or tab block
No tab block or PCA
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The number of women who will feel less pain post CS
Time Frame: 2 days
|
the degree of pain that will be felt post CS
|
2 days
|
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)
May 28, 2020
Primary Completion (ACTUAL)
March 15, 2021
Study Completion (ACTUAL)
April 1, 2021
Study Registration Dates
First Submitted
May 23, 2020
First Submitted That Met QC Criteria
May 23, 2020
First Posted (ACTUAL)
May 28, 2020
Study Record Updates
Last Update Posted (ACTUAL)
May 25, 2021
Last Update Submitted That Met QC Criteria
May 21, 2021
Last Verified
May 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- tab block
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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