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Clinical Trials in Turkey / NCT07166874
Recruiting Not applicable

The Impacts of Gluten-free Diet in Patients With Ankylosing Spondylitis

NCT07166874 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-01-31
Last updated
2025-09-10

Condition(s) studied

Ankylosing Spondylitis

Investigational drug(s) / intervention(s)

Gluten Free Diet

Gluten Free Diet: Patients in the experimental arm will received a gluten-free diet for 8 weeks.

Study summary

Subclinical intestinal inflammation and intestinal permeability have been reported in patients with ankylosing spondylitis. Gluten is one of the main triggers of zonulin releaseand gluten intake may contribute to the development of the disease by increasing intestinal permeability. This study aims to determine the impacts of a gluten-freediet on intestinal permeability, sub-clinical intestinal inflammation, disease activity, functional status and quality of life in patients with ankylosing spondylitis. The main questions it aims to answer are:

Does a gluten-free diet have an effect on disease activity and functional status in patients with ankylosing spondylitis? Does a gluten-free diet have an effect on intestinal permeability and subclinical intestinal inflammation in patients with ankylosing spondylitis? The investigators will evaluate the effects of the gluten-free diet compared to a control group.

Eligibility

Sex
ALL
Min age
18 Years
Max age
64 Years
Healthy volunteers
No
Inclusion Criteria: * diagnosis of axial SpA defined by ASAS criteria * Adults (aged 18-64 years) * stable treatment (NSAID and/or DMARD) for at least 3 months * provide written informed consent and submit to the requirements of the study Exclusion Criteria: * Any diet at the time of inclusion or within 3 months prior to inclusion; * have a history of celiac disease; * have a history of Ulcerative Colitis, Crohn's Disease and Irritable Bowel Syndrom * patients with Type 1 and Type 2 Diabetes Mellitus * patients with Hashimoto Thyroiditis * are pregnant, breastfeeding, * patients who have used omega-3 and vitamins (A, C, E) regularly in the last 3 months. * BMI \<18,50 kg/m2 * BMI ≥29,99 kg/m2

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
Bakırköy Dr. Sadi Konuk Training and Research hospital Istanbul Turkey (Türkiye) Recruiting
İstanbul Medeniyet University Istanbul Turkey (Türkiye) Active Not Recruiting
İstanbul Sağlık Bilimleri University Istanbul Turkey (Türkiye) Active Not Recruiting
Marmara University Istanbul Turkey (Türkiye) Active Not Recruiting

More Saglik Bilimleri Universitesi trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07166874 on ClinicalTrials.gov ↗ ← All trials in Turkey