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NCT06923696
Low FODMAP Diet and Gluten Free Diet in IBS
NA trial testing Diet therapy in IBS - Irritable Bowel Syndrome in 75 participants. Completed in 9 September 2024.
25 August 2024
Quick facts
| Lead sponsor | Nuh Naci Yazgan University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 75 |
| Start date | 27 July 2023 |
| Primary completion | 25 August 2024 |
| Estimated completion | 9 September 2024 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Diet therapy
Conditions studied
- IBS - Irritable Bowel Syndrome — all drugs for IBS - Irritable Bowel Syndrome →
- Diet, Healthy — all drugs for Diet, Healthy →
- Elimination Disorder With Fecal Symptoms — all drugs for Elimination Disorder With Fecal Symptoms →
Sponsor
Nuh Naci Yazgan University
Who can join
Adults 18 to 65, any sex, with IBS - Irritable Bowel Syndrome or Diet, Healthy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The data of the research will be collected from patients who have applied to the Gastroenterology Polyclinic of Kayseri City Hospital or have previously been diagnosed with Irritable Bowel Syndrome (IBS). The data will be collected through face-to-face interviews using a questionnaire form. Participation in the study is entirely voluntary, and participants have the right to withdraw from the research at any time if they wish. The general flowchart of the research is shown in Figure 1. Figure 1. Flowchart of the Research Patients with IBS applying to the Gastroenterology Polyclinic: According to Rome IV criteria, individuals aged between 19-64, with BMI \>18.5 and \<29.9 kg/m2, non-cancerous, not using probiotics in the last month, and not following a gluten-free diet. Interview Group 1: Low FODMAP diet Group 2: Gluten-free diet Socio-demographic characteristics, general dietary habits, level of physical activity, anthropometric measurements, body composition analysis, IBS-SSS, IBS-QOL, IBS-VAS, Bristol Stool Scale, 24-hour retrospective food consumption record, Food Frequency Questionnaire. Second Interview (after 4 weeks) Anthropometric measurements, body composition analysis, IBS-SSS, IBS-QOL, IBS-VAS, Bristol Stool Scale, 3-day retrospective food consumption record.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06923696
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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- NCT06215222 — Capsule Microbiota Sampling in IBS/Functional Gastrointestinal Disease · recruiting
- NCT05815602 — Ebastine Versus Mebeverine in IBS Patients · Phase 3 · recruiting
Other Nuh Naci Yazgan University trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06923696 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Nuh Naci Yazgan University
- Last refreshed: 11 April 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06923696.
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