Chronic Pain Clinical Trial
Official title:
Prevalence and Risk Factors for Chronic Pain After Cesarean Delivery in Upper Egypt: Retrospective Study
NCT number | NCT04810767 |
Other study ID # | 2020 |
Secondary ID | |
Status | Not yet recruiting |
Phase | |
First received | |
Last updated | |
Start date | May 2023 |
Est. completion date | December 2024 |
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
Status | Not yet recruiting |
Enrollment | 100 |
Est. completion date | December 2024 |
Est. primary completion date | October 2024 |
Accepts healthy volunteers | |
Gender | Female |
Age group | 20 Years to 40 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Bahaa Mohammed Refaie |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Chronic pain | Pain experienced assessed by questionnaire described by Nikolajsen et al, 2004 | Three months after the last ceserean section |
Status | Clinical Trial | Phase | |
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Completed |
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