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The Effect of Jiangwei Anzhong Decocotion on Treating Gastroesophageal Reflux Disease with Liver Stomach Stasis Heat Type Based on Brain Intestinal Peptide: Study Protocol for a Randomized Controlled Trial

A Randomized Controlled Study on the Treatment of Gastroesophageal Reflux Disease with Stagnated Heat in Liver and Stomach by Jiangwei Anzhong Decoction Based on Brain-gut Peptide

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074154
Enrollment
Unknown
Registered
2023-07-31
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-08-07

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

Conditions

Gastroesophageal reflux disease

Interventions

experimental group:Take Jiangwei Anzhong Decoction
Control group:Take Rabeprazole

Sponsors

Fangshan Hospital of Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Western medical diagnosis is consistent with GERD; (2) Chinese medicine diagnosis of Stagnated Heat in Liver and Stomach; (3) Those who are between 18-75 years old; (4) Those who voluntarily participated and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) Undiagnosed GERD, Chinese medicine identification is not Stagnated Heat in Liver and Stomach; endoscopic diagnosis of BE patients; (2) Recent history of taking medications that affect the gastrointestinal tract, such as glucocorticoids, aspirin, and calcium antagonists; (3) Combined organic upper gastrointestinal tract gastrointestinal disease (gastric ulcer, gastric cancer, etc.), primary esophageal dyskinesia; (4) Those with comorbid serious primary diseases of other systems; (5) Those with a history of surgery in the gastroesophageal area; (6) Pregnant and lactating women, and patients with disabilities (blindness, deafness, mute, intelligence, mental retardation, etc.) as defined by law; (7) Those with allergy, intolerance or contraindication to the drugs involved in this trial; (8) Patients who are also participating in clinical trials of other drugs;

Design outcomes

Primary

MeasureTime frame
serum 5-hydroxytryptamine(5-HT);serum VIP;

Secondary

MeasureTime frame
GerdQ Scale;Chinese Medicine Symptoms ClinRO Evaluation Scale;Self-Rating Anxiety Scale(SAS);Self-Rating Depression Scale(SDS);

Countries

China

Contacts

Public ContactBoyi Jia

Fangshan Hospital of Beijing University of Chinese Medicine

jiaboyiwilliam@163.com+86 156 0005 2896

Outcome results

None listed

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