Skip to content

Lotus Leaf Extracts for Chronic Atrophic Gastritis: a Multi-center, Randomized, Double-blind, Placebo-Controlled Trial

Lotus Leaf Extracts for Chronic Atrophic Gastritis: a Multi-center, Randomized, Double-blind, Placebo-Controlled Trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039549
Enrollment
Unknown
Registered
2020-10-31
Start date
2020-11-01
Completion date
Unknown
Last updated
2021-02-08

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

Conditions

Chronic Atrophic Gastritis

Interventions

Treatment:Lotus Leaf Treatment
Placebo:Placebo

Sponsors

Tsinghua University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 18 and 70 years. 2.Patients with chronic atrophic gastritis by endoscopic and pathology.

Exclusion criteria

Exclusion criteria: 1.Patients with gastric ulcer,gastric polyps,gastroesophageal reflux or history of stomach surgery. 2.Having taken glucocorticoid or non-steroidal anti-inflammatory drugs in the past three months. 3.Patients with cardiovascular diseases,respiratory system, digestive system or endocrine systems . 4.Significant renal or hepatic insufficiency (defined as a serum creatinine concentration, alanine aminotransferase, or aspartate minotransferase value that is twice greater than the upper limit of normal). 5.Allergic to lotus leaf related food or drug. 6.Pregnancy or to be pregnancy;lactating women. 7.Other conditions that render outcomes or follow-up unlikely to be assessed. 8.Tumors or other serious life-threatening illness,expected lifetime less than 12 months. 9.Having participated in other drug trials in the past three months.

Design outcomes

Primary

MeasureTime frame
Difference in the Correa scores between baseline and 12 months follow-up;

Secondary

MeasureTime frame
Difference in the Correa scores between baseline and 6 months follow-up;Change of OLGA\OLGIM stages in 6 months and 12 months.;Difference in the updated Sydney system scores in 12 months;Appearance rate of high-grade dysplasia;Change of serum level of pepsinogen and Gastrin;Rate of symptom improvement;

Countries

China

Contacts

Public ContactLi Shao

Tsinghua University

shaoli@mail.tsinghua.edu.cn+86 10 62797035

Outcome results

None listed

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