A Prospective Evaluation of Hemorrhoidal Surgery Outcome in Istanbul
NCT ID: NCT05429060
Last Updated: 2022-06-23
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
2000 participants
OBSERVATIONAL
2022-06-01
2024-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Hemorrhoidal surgery
All surgical interventions under general or local anesthesia, either in the office or operation room, including any type of injection, excision, ligation, ablation, mucopexy and suturation.
Eligibility Criteria
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Inclusion Criteria
* Elective or emergency interventions (including thrombectomy)
* Surgical interventions in operation room or office
* Any kind of excision, sclerotherapy, ligation, suturation, ablation, mucopexy
Exclusion Criteria
* Previous surgery for hemorrhoids (any intervention other than medical treatment)
* Previous perianal surgery (internal sphincterotomy, fistula surgery)
* Pelvic and/or perineal radiotherapy
* Previous obstetric or perianal injury and/or sphincter repair
* Previous rectal surgery (distal colectomy for benign or malignant etiology)
18 Years
ALL
No
Sponsors
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Istanbul Medipol University Hospital
OTHER
Responsible Party
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Principal Investigators
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Naciye Cigdem Arslan, MD
Role: STUDY_DIRECTOR
Medipol University
Locations
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Medipol University Bahcelievler Hospital
Istanbul, Bahcelievler, Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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E-10840098-772.02-109
Identifier Type: -
Identifier Source: org_study_id
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