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Clinical Discussion Program for Moderate Acid Suppression in Gastroesophageal Reflux Disease

Clinical Discussion Program for Moderate Acid Suppression in Gastroesophageal Reflux Disease

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088259
Enrollment
Unknown
Registered
2024-08-14
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Gastro-oesophageal reflux disease

Interventions

Standard dose group:Tegoprazan 50mg/day
RE grade A~B, oral administration for 4 weeks
RE grade C~D, oral administration for 8 weeks
Low-dose group:Tegoprazan 50mg, once every other day, RE grade A~B, oral administration for 4 weeks

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: GERD is defined as having heartburn symptoms 1 time per week, endoscopic diagnosis of reflux esophagitis grade A~D, age 18~65 years.

Exclusion criteria

Exclusion criteria: hiatal hernia, Barrett's esophagus; peptic ulcer; various malignant tumors; heart, liver, kidney, pulmonary insufficiency; pregnancy,in perinatal and lactating women; patients with chronic diseases such as endocrine and metabolic diseases and psychiatric diseases

Design outcomes

Primary

MeasureTime frame
Healing rate of esophageal mucosal lesions;

Secondary

MeasureTime frame
Gastrin-17;Pepsinogen;Pepsin;Pancreatic Exocrine Function;Small Intestinal Bacterial Overgrowth;

Countries

China

Contacts

Public ContactZhiyin Huang

Department of Gastroenterology and Hematology, West China Hospital, Sichuan University

huang-zhiyin@qq.com+86 158 2818 4989

Outcome results

None listed

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