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Therapeutic Efficacy of Fu's Subcutaneous Needling for Chronic Atrophic Gastritis and Its Effects on Serum PGI, PGII, and G-17 Levels

Therapeutic Efficacy of Fu's Subcutaneous Needling for Chronic Atrophic Gastritis and Its Effects on Serum PGI, PGII, and G-17 Levels

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000249
Enrollment
Unknown
Registered
2026-02-03
Start date
2025-12-19
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

chronic atrophic gastritis

Interventions

Fu's Subcutaneous Needling Group:Fu's Subcutaneous Needling therapy will be administered. Disposable FSN needles (Model M, Nanjing Paifu Medical Technology Co., Ltd.) will be used. During each session
Active Drug Control Group (Wei Fu Chun Capsule):Oral administration of Wei Fu Chun Capsules (Hangzhou Huqingyutang Group Co., Ltd., 0.35g/capsule). The dosage is 4 capsules, three times daily. The tre

Sponsors

Nanjing Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients meeting the diagnostic criteria for Chronic Atrophic Gastritis (CAG). 2. Helicobacter pylori (H. pylori)-negative status, or a documented history of H. pylori infection with successful eradication therapy completed at least six months prior to enrollment and no evidence of current infection. 3. Age between 18 and 65 years, inclusive. 4. Willingness to participate in the study and provision of written informed consent.

Exclusion criteria

Exclusion criteria: 1. History of prior gastric surgery. 2. Regular use of medications that may influence gastric physiology or the study outcomes, including proton pump inhibitors, H2 receptor antagonists, or gastric mucosal protective agents. 3. Presence of significant comorbid conditions that could confound study assessments, such as severe hematologic, hepatic, cardiac, or renal diseases, or active malignancy. 4. Pregnant or lactating individuals.

Design outcomes

Primary

MeasureTime frame
Gastric Mucosa Histopathology Score;

Secondary

MeasureTime frame
Effective Rate of Gastric Mucosa Improvement;Traditional Chinese Medicine Symptom Score;Effective Rate of Traditional Chinese Medicine Syndrome Improvement;Serum Assessment Parameters;

Countries

China

Contacts

Public ContactSHI Juanjuan

Nanjing Hospital of Chinese Medicine

df_sjj@163.com13813897286

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026