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Comparative clinical studies to evaluate the efficacy and safety of gastritis after Hwangryunhaedok-tang with gastritis

A comparative clinical trial to evaluate the efficacy and safety of 'Hwangryenhaedogtang‘ in treatment of gastritis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004052
Enrollment
20
Registered
2019-06-12
Start date
2019-04-02
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

None listed

Interventions

Drug : All subjects will take 2 capsulus of Hwangryunhaedok-tang(Redoxin Cap.), 3 times a day, 30 minutes after meals, for 8 weeks.

Sponsors

Pusan National University Korean Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Only those aged 19 or over but under 65 2) Body mass index (BMI) of more than 25 kg / m2 3) Those who have been diagnosed with gastritis by gastroscopy 4) After fully hearing and understanding the details of this clinical trial, you agree to participate voluntarily and agree in writing to abide by the instructions. 5) Those who can follow up during the clinical trial

Exclusion criteria

Exclusion criteria: 1) Those who can not undergo gastroscopy 2) peptic ulcer (except patients with scarring) 3) Those who have had past gastric acid secretion surgery or stomach and esophagus surgery 4) A person with a history of gastrointestinal malignancies 5) In the second week prior to administration of test drug, H2 receptor antagonist, anticholinergic agent (muscarinic receptor antagonist), gastrin receptor antagonist, prostaglandin agent, proton pump inhibitor, gastric mucosal protective agent, One who took it 6) Those who need to continue taking medications that may affect this test, such as corticosteroids, non-steroidal anti-inflammatory drugs, and aspirin 7) Those taking thrombolytic agents (such as cerebral thrombosis, myocardial infarction, thrombophlebitis), consuming coagulation disorder patients and antithrombotic agents such as warfarin 8) People with Zollinger-Ellison syndrome 9) Those with a history of drug allergy symptoms (rash, fever, itching, etc.) 10) Patients with abnormal liver function and renal function with serum AST, ALT and creatinine> 3 times the normal peak 11) Those who have serious obstacles such as liver, kidney, heart, lung, blood 12) Those who are pregnant or breastfeeding, those who are pregnant, those who have a pregnancy plan or do not agree to the appropriate method of contraception 13) Those who have severe mental illnesses such as depression, anxiety disorder, or are currently taking psychotropic drugs such as antidepressants 14) Drug or alcohol addict 15) Those taking medicines or health functional foods that may affect the clinical trial 16) Smokers whose average daily smoking amount exceeds 10 per day during the past 3 months 17) Those who continue to drink (21 units / week, 1 unit = 10 g of pure alcohol) Example> Beer 5 ° 1 cup (250 ml) = 10 g, soju 20 ° 1 cup (50 ml) = 8 g, wine 12 ° 1 cup (125 ml) = 12 g 18) Any person judged by the examiner to be inappropriate for other examinations

Design outcomes

Primary

MeasureTime frame
the improvement rates of gastritis symptoms

Secondary

MeasureTime frame
Body composition test

Countries

Korea, Republic of

Contacts

Public ContactHeeyeon Kim

Pusan National University Korean Medicine Hospital

kimhy1872@daum.net+82-55-360-5575

Outcome results

None listed

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