Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
100 participants
OBSERVATIONAL
2023-05-31
2024-12-31
Brief Summary
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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
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Interventions
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Questionnaire
Pain experienced assessed by questionnaire described by Nikolajsen et al, 2004
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
20 Years
40 Years
FEMALE
No
Sponsors
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Bahaa Mohammed Refaie
OTHER
Responsible Party
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Bahaa Mohammed Refaie
Lecturer of anesthesia and ICU
Principal Investigators
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Kareem ElGebaly, Lecturer
Role: STUDY_CHAIR
Lecturer of anesthesia and ICU
Hossam Eldin Mostafa, Consultant
Role: STUDY_DIRECTOR
Consultant of anesthesia and ICU Elhelal insurance hospital
Central Contacts
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Other Identifiers
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2020
Identifier Type: -
Identifier Source: org_study_id
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