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Study on efficacy and safety of human umbilical cord-derived mesenchymal stem cells therapy for chronic atrophic gastritis

Study on efficacy and safety of human umbilical cord-derived mesenchymal stem cells therapy for chronic atrophic gastritis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046372
Enrollment
Unknown
Registered
2021-05-15
Start date
2021-06-01
Completion date
Unknown
Last updated
2021-12-21

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

Conditions

chronic atrophic gastritis

Interventions

experimental group:submucosal injection of human umbilical cord-derived mesenchymal stem cells
Control group:submucosal injection of saline

Sponsors

Shandong Provincial Hospital Affiliated to Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Volunteer to participate in the trial and sign an informed consent form; 2. Aged 18 to 65 years, regardless of gender; 3. Patients diagnosed as chronic atrophic gastritis (with or without intestinal metaplasia) under endoscopy and pathology; 4. Patients whose C13 breath test is negative or positive in the past have now eradicated Hp; 5. Patients without contraindications to submucosal injection of cord blood stem cells.

Exclusion criteria

Exclusion criteria: 1. Patients suffering from gastric ulcer, erosive gastritis, active upper gastrointestinal bleeding, gastric varices or other gastric tumors; 2. Patients who are taking or have taken proton pump inhibitors, antibiotics, glucocorticoids, non-steroidal anti-inflammatory drugs, immunosuppressants and other drugs in the past six months; 3. Those who have undergone gastric surgery or those who need gastric surgery during the study period; 4. Patients with severe systemic diseases (cardio-cerebrovascular disease, liver disease, blood, kidney, lung or liver disease); 5. Pregnant or lactating female patients; 6. Patients who are unwilling to undergo repeated endoscopic examinations and treatments.

Design outcomes

Primary

MeasureTime frame
Histopathological scoring of gastric mucosal;

Secondary

MeasureTime frame
Gastric mucosa OLGA & OLGIM rating;Gastrin-17;Pepsinogen II/I;

Countries

China

Contacts

Public ContactXu Hongwei

Shandong Provincial Hospital Affiliated to Shandong First Medical University

xhwsdslyy@sina.com+86 15168889328

Outcome results

None listed

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