- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04810767
Chronic Pain After CS in Egypt
Prevalence and Risk Factors for Chronic Pain After Cesarean Delivery in Upper Egypt: Retrospective Study
This retrospective study will include Women who will attending to Azhar assuit, Sohag and South valley universities hospitals for any reason in the duration from 1 May to 31 October 2021, and who underwent elective CD under spinal anesthesia with horizontal lower abdominal surgical incision within last two years.
Exclusion criteria will be refusal to participate, age less than 18 years, recent CD (within 3 months), if the infant had died, and history of chronic pain medications or psychiatric disorder.
Data collection
Participants will be contacted personally by one of study authors. Data collected are consisted of:
- Participants' characteristics as Age, parity and ways of delivery, weight, height, residency, husband smoking status, work, previous abdominal surgery, history of diabetes mellitus and hypertension.
- Last CD related data which include presence of multiple pregnancies, if CD was in private/public facility, presence surgical wound infection.
- Pain experienced will be assessed by questionnaire described by Nikolajsen et al, 2004
Study Overview
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Bahaa M Refaie, Lecturer
- Phone Number: 00201026887257
- Email: bahaarefaay@med.sohag.edu.eg
Study Contact Backup
- Name: Mohammed A Soliman
- Email: Mohammedsoliman@med.svu.edu.eg
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Women attending to Azhar assuit, Sohag and South valley universities hospitals for any reason in the duration from 1 May to 31 October 2021, and who underwent elective ceserean section under spinal anesthesia with horizontal lower abdominal surgical incision within last two years
Exclusion Criteria:
- refusal to participate, age less than 18 years, recent ceserean section (within 3 months), if the infant had died, and history of chronic pain medications or psychiatric disorder
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Chronic pain
Time Frame: Three months after the last ceserean section
|
Pain experienced assessed by questionnaire described by Nikolajsen et al, 2004
|
Three months after the last ceserean section
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Kareem ElGebaly, Lecturer, Lecturer of anesthesia and ICU
- Study Director: Hossam Eldin Mostafa, Consultant, Consultant of anesthesia and ICU Elhelal insurance hospital
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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