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Study identifier: NCT07385196 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Defining Ileorectal Syndrome: a Prospective Observational Study

Condition: Total Colectomy · Diarrhea · Urgency Incontinence  ·  Sponsor: Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital

PhaseN/A
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

1. Study Title: Trying to Define Ilorectal Syndrome: A Prospective Observational Study 2. Study Objective and Significance: Primary Objective: To prospectively evaluate the frequency, symptom severity, and impact on quality of life of ileorectal syndrome developing in patients who have undergone total colectomy and ileorectal anastomosis. Secondary Objectives: * To examine the relationship between postoperative bowel dysfunction and quality of life * To investigate clinical factors affecting symptom severity This study aims to contribute to postoperative follow-up and management strategies by revealing patient-centered outcomes of ileorectal syndrome. 3. Expected Benefits and Risks of the Study: Expected Benefits * Prospective and systematic evaluation of ileorectal syndrome * Identification of factors affecting the quality of life of these patients * Increased awareness in clinical follow-up Potential Risks * The study is observational and questionnaire-based and does not involve additional medical risks * No invasive procedures will be performed on the patients 4. Type, scope, and design of the planned study: * Type: Prospective, observational * Scope: Single-center * Design: Questionnaire-based clinical trial 5. Number of patients and volunteers to be included in the study, their qualifications, and the rationale for selection: * Total number of patients: 30 * Age range: ≥18 years * Gender: Female and male This numbe…

This description comes directly from the study's public registry record.

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Locations (1)

general surgery clinic(Gazi Yaşargil Tr and Res HospitalDiyarbakır, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07385196