A Prospective Evaluation of Hemorrhoidal Surgery Outcome in Istanbul

NCT ID: NCT05429060

Last Updated: 2022-06-23

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

2000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-06-01

Study Completion Date

2024-05-31

Brief Summary

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This study aims to evaluate the effect of surgical treatments on the quality of life in hemorrhoidal disease. All available treatment methods will be included in this 1-year cohort which is going to collect data from a big metropol.

Detailed Description

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Conditions

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Hemorrhoids Quality of Life Complication of Treatment Indication, Unlabeled

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Surgical interventions under local and/or general anesthesia
* Elective or emergency interventions (including thrombectomy)
* Surgical interventions in operation room or office
* Any kind of excision, sclerotherapy, ligation, suturation, ablation, mucopexy

Exclusion Criteria

* Any accompanying perianal disease (anal fistula, anal fissure, perianal abscess, anal condyloma extending into the anal canal)
* 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)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul Medipol University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Naciye Cigdem Arslan, MD

Role: CONTACT

+905313890975

Facility Contacts

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Osman Civil, MD

Role: primary

+905058334286

Nevin Sakoglu, MD

Role: backup

+905333741297

Other Identifiers

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E-10840098-772.02-109

Identifier Type: -

Identifier Source: org_study_id

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