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A randomized controlled unblinded clinical study on the treatment of gastroesophageal reflux disease (GERD) with Tegoprazan versus Qishi Shengjiangguiyuan granule

A study of the clinical efficacy of Tegoprazan in the treatment of gastroesophageal reflux disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006461
Enrollment
Unknown
Registered
2022-08-12
Start date
2022-08-10
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

gastroesophageal reflux disease

Interventions

Treatment Group:Tegoprazan
Control Group:Qishi Shengjiangguiyuan granule

Sponsors

Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 70. 2. Meet the diagnostic criteria for gastroesophageal reflux disease in the guidelines for primary care (2019). 3. Sign a written informed consent and be willing to comply with all research procedures.

Exclusion criteria

Exclusion criteria: 1. Patients with other organic lesions of esophagus and gastrointestinal tract confirmed by endoscopy, these include previous total subtotal gastrectomy, esophageal stricture, achalasia, stomach or peptic ulcer, acute gastritis, Zollinger-ellison syndrome, inflammatory bowel disease, etc. 2. Current use of H2 receptor antagonist, antacids, gastrointestinal stimulants or steroids, and a history of sensitivity to PPI medications. 3. Patients with severe primary diseases, history of malignancy, or psychosis, such as cardio-cerebral vascular disease, liver disease, kidney disease, etc. 4. Persons under the age of 18 and over 70 years or pregnant or lactating women (women of reproductive age who were not pregnant before enrolment and who had used effective contraception during the course of the study may be enrolled) ; Participants in other studies within 30 days of using the study drug; alcohol and/or drug abuse (addiction or dependence) or poor adherence to the physician's judgment.

Design outcomes

Primary

MeasureTime frame
GerdQ;FSSG;

Countries

China

Contacts

Public ContactTao Zhang

Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine

327664246@qq.com13788403729

Outcome results

None listed

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