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Evaluating the effect of administration of Lactocare® probiotic on gasterointestinal symptoms and Anti-Ttg antibody in patients with celiac disease: Randomized controlled Clinical trial

Evaluating the effect of administration of Lactocare® probiotic on gasterointestinal symptoms and Anti-Ttg antibody in patients with celiac disease: Randomized controlled Clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20080921001264N12
Enrollment
98
Registered
2023-01-24
Start date
2023-01-20
Completion date
Unknown
Last updated
2023-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

celiac disease. Celiac disease

Interventions

Intervention 1: Intervention group: Including 49 patients, they will use 2 capsules of Lactocar probiotic every day for 6 weeks, with an interval of 12 hours, and along with this medicine, they will f

Sponsors

Gorgan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Confirmation of celiac disease with small intestine biopsy Measurement of antibody titer against tissue transglutaminase (Anti TTg) Age above 18 years

Exclusion criteria

Exclusion criteria: Any recent infections Concomitant inflammatory bowel disease (IBD) Immune deficiency (acquired or non-acquired) Taking drugs that affect the immune system (immune suppressors and stimulants) Recent GI surgery Taking NSAID painkillers or antibiotics in the last 6 weeks Having cancer or being HIV positive Cardiovascular diseases, glands, kidney, liver, neurological or mental malignancy Pregnancy and breastfeeding Alcohol and drug addiction Participation in another similar study within the last 6 months unwillingness to take probiotics patient being out of reach

Design outcomes

Primary

MeasureTime frame
The severity and extent of disease symptoms. Timepoint: The beginning of the study and 6 weeks after the start of the study. Method of measurement: CSI ( celiac symptom index ) questionnaire.;Tissue transglutaminase antibody titer (Anti-Ttg). Timepoint: The beginning of the study and 6 weeks after the start of the study. Method of measurement: titer Anti-TTG.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTaghi Amiriani

Gorgan University of Medical Sciences

s_besharat_gp@yahoo.com+98 17 3225 1910 ext. 2637

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026