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Clinical Trial Summary

The primary aim of the current study is to evaluate and compare 6-month complication rates after thrombectomy and local excision treatments. The investigators aim to compare thrombectomy and local excision treatments in many different aspects: - The investigators will follow these patients for 6 months by scheduling follow-up visits (or by phone if the patient cannot attend) 4 times during this period (1st week, 1st month, 3rd month, 6th month). - The investigators will examine bleeding, pain, anal stricture/stenosis, infection, time until return to normal daily activity, relapse and incontinence after treatment - To assess quality of life outcomes, the investigators use the 36-Item Short Form Health Survey (SF-36). These measures rely upon patient self-reporting and are utilized for routine monitoring and assessment of care outcomes in patients. - The investigators will use the Wexner incontinence score for assessment of incontinence. In each hospital, medical students, residents and surgeons can be involved in the study. In the following 6-month period, all collaborators will be collecting the data of the patients who have been operated for external hemorrhoids via the thrombectomy or local excision procedures.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03903536
Study type Observational [Patient Registry]
Source Gazi University
Contact
Status Completed
Phase
Start date September 1, 2020
Completion date June 1, 2022

See also
  Status Clinical Trial Phase
Completed NCT00717782 - Pain Relief for Thrombosed External Haemorrhoids Phase 4