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Clinical Trial of Gut Microbiota in the Management of Immune Thrombocytopenia

A Multi-center Randomized Clinical Trial of Regulating Gut Microbiota by Probiotic Agents in Management of Immune Thrombocytopenia

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03033199
Enrollment
60
Registered
2017-01-26
Start date
2017-01-31
Completion date
2018-08-31
Last updated
2017-01-26

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

Conditions

Immune Thrombocytopenia

Keywords

Gut microbiota, Immune thrombocytopenia

Brief summary

Primary immune thrombocytopenia (ITP) is an acquired autoimmune bleeding disorder, accounting for about 1/3 of clinical hemorrhagic diseases. Loss of immune tolerance leading to increased platelet destruction and decreased platelet production is the main pathogenesis of ITP. Dysbiosis of the gut microbiota was found in many autoimmune diseases like rheumatic arthritis(RA),inflammatory bowel disease(IBD),multiple sclerosis and probiotic treatment or fecal microbiota transplantation(FMT) which can regulate the gut microbiota has good clinical efficacy in those disorders. One ITP patient with ulcerative colitis(UC) was treated with FMT and got progressive but significant increase in platelet level and lasted for several years.

Detailed description

The investigators are undertaking a multicenter, single-arm study of 60 primary ITP adult patients from 5 medical centers in China. All the participants are randomly divided into two groups to orally intake either probiotic supplements (n = 30) or placebo (n = 30) for 4 weeks in addition with high dose dexamethasone(40 mg/d for 4 days). Platelet count, bleeding and other symptoms were evaluated before and after treatment. Adverse events are also recorded throughout the study.

Interventions

probiotic capsules containing three viable and freezedried strains-Lactobacillus acidophilus,Lactobacillus casei, and Bifidobacterium bifidum:2 capsules, bid x 4 weeks for one cycle. It will be given for one or two cycles.

DRUGDexamethasone

Dexamethasone 40 mg per day, 4 consecutive days

Sponsors

Jinan Central Hospital
CollaboratorOTHER
The Second Hospital of Shandong University
CollaboratorOTHER
Qianfoshan Hospital
CollaboratorOTHER
Qingdao University
CollaboratorOTHER
Yantai Yuhuangding Hospital
CollaboratorOTHER
Shandong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* need of treatment(s) (including, but not limited to, low dose of corticosteroids) to minimize the risk of clinically significant bleeding. Need of on-demand or adjunctive therapy alone does not qualify the patient as refractory * primary ITP confirmed by excluding other supervened causes of thrombocytopenia

Exclusion criteria

* pregnancy * hypertension * cardiovascular disease * diabetes * liver and kidney function impairment * HCV, HIV, HBsAg seropositive status * patients with systemic lupus erythematosus and/or antiphospholipid syndrome * patients with known gastro-intestinal bleeding. * use of antibiotics, prebiotics or probiotics in the past 4 weeks;

Design outcomes

Primary

MeasureTime frameDescription
Platelet countFrom date of randomization until the date of first documented progression,up to 12 monthsR. A response (R) was defined as a sustained (≥ 3 months) platelet count ≥ 30×10\^9/L without recurrence of thrombocytopenia

Countries

China

Contacts

Primary ContactMing Hou
houming@medmail.com.cn

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026