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Effect and mechanism of probiotics in adjuvant treatment of reflux esophagitis

Effect and mechanism of probiotics in adjuvant treatment of reflux esophagitis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059624
Enrollment
Unknown
Registered
2022-05-04
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

reflux esophagitis

Interventions

Case group:Oral probiotics
Case group2:Oral placebo

Sponsors

The First Hospital of Nanchang
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Agree to accept esomeprazole treatment, have not received PPI before or stop PPI treatment for at least 1 month, aged 18-65 years; 2. Patients who have not taken antibiotics, probiotics, lactulose, other antacids or drugs that increase gastrointestinal motility or have received enema; 3. Liver and kidney functions are normal.

Exclusion criteria

Exclusion criteria: 1. Liver cirrhosis, kidney damage, tumor, thyroid disease, diabetes, Crohn's disease or ulcerative colitis; 2. Diarrhea, malabsorption and constipation caused by hiatal hernia, esophageal stricture, liver, gallbladder and pancreatic diseases; 3. History of gastrointestinal or abdominal surgery; 4. Pregnant or lactating women; Patients receiving immunosuppressive therapy; 6. Patients diagnosed as irritable bowel syndrome (IBS) according to RomeIII criteria, or patients who do not meet the diagnostic criteria but have persistent abdominal distension, diarrhea or constipation within = 3 months; 7. Severe cardiopulmonary insufficiency, significantly abnormal bleeding and clotting time (PT, APTT); 8. Those who cannot take orally or are allergic to probiotics; 9. The researcher believes that it is not suitable to participate in the clinical trial; 10. Those who have participated in clinical research of other drugs in the past three months.

Design outcomes

Primary

MeasureTime frame
clinical symptoms;Endoscopy;Inflammatory cytokines;Intestinal microecological analysis;

Countries

China

Contacts

Public ContactNian Fan

The First Hospital of Nanchang

fnian3893@126.com+86 13970053893

Outcome results

None listed

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