Skip to content

Yiwei Jiaohuang Ointment for Gastrointestinal Bleeding Associated With Oral Antithrombotic Agents

Yiwei Jiaohuang Ointment for Gastrointestinal Bleeding Associated With Oral Antithrombotic Agents: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07339956
Enrollment
60
Registered
2026-01-14
Start date
2026-01-10
Completion date
2026-08-30
Last updated
2026-01-26

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

Conditions

Gastrointestinal Bleeding

Keywords

Antithrombotic therapy, Traditional Chinese Medicine

Brief summary

The goal of this clinical trial is to evaluate the clinical efficacy and safety of YiWei Jiaohuang Ointment in treating gastrointestinal bleeding associated with oral antithrombotic therapy. The main question it aims to answer is: Does Yiwei JiaoHuang Ointment accelerate the conversion to negative results in fecal occult blood tests among patients with gastrointestinal bleeding associated with antithrombotic therapy? Researchers will compare use rabeprazole alone as routine therapy to see if Yiwei JiaoHuang Ointment can accelerate the conversion to negative results in fecal occult blood tests. Participants will : Take Yiwei JiaoHuang Ointment every day for 2 weeks. Return to the hospital for a fecal occult blood test after 3 days, 1 week, and 2 weeks of medication.

Interventions

DRUGA Chinese herb formula--Yiwei Jiaohuang Onitment

Yiwei Jiaohuang Onitment consists of four Chinese herbs: 3g of Duyiwei(Lamiophlomis Herb), 3g of raw Da Huang(Rhubarb Root and Rhizome (Unprocessed)), 6g of Bai Ji(Bletilla Rhizome) and 10g of Ejiao (donkey-hide gelatin). Prepared as ointment, patients should take one dose daily in the morning on an empty stomach for 2 weeks.

DRUGRabeprazole Enteric-Coated Tablets

Rabeprazole Enteric-Coated Tablets10mg once a day for 2 weeks

Sponsors

China-Japan Friendship Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Oral therapy with at least one antiplatelet or anticoagulant agent, including: aspirin, clopidogrel, ticagrelor, prasugrel, warfarin, rivaroxaban, apixaban, edoxaban, dabigatran, etc.; * BARC stage 1 or 2; * Traditional Chinese Medicine pattern identified as phlegm-heat and blood stasis obstruction syndrome; * Age 18-90 years; * Signed informed consent.

Exclusion criteria

* Patients with gastrointestinal bleeding resulting in hemoglobin levels \<20 g/L and/or requiring hospitalization; * Gastrointestinal malignancies; * Cases where the source of occult blood cannot be distinguished, such as fresh bleeding from hemorrhoids; * Concurrent use of hemostatic traditional Chinese medicine preparations like Yunnan Baiyao; * Significant liver or kidney dysfunction, with ALT, AST, or serum creatinine exceeding three times the upper limit of normal; * Pregnant women, women planning pregnancy, or lactating women; * Individuals deemed unsuitable for this clinical trial by the investigator.

Design outcomes

Primary

MeasureTime frame
The rate of negative fecal occult blood test results in the two groups of patients after 2 weeks of intervention.two weeks of intervention

Secondary

MeasureTime frame
Time required for fecal occult blood to turn negative in two groups of patients.two weeks of intervention
The rate of negative fecal occult blood test results in the two groups of patients after 3 days of intervention.3 days of intervention
The rate of negative fecal occult blood test results in the two groups of patients after one week of intervention.one week of intervention
Changes in hemoglobin levels in two groups of patients after 2 weeks of intervention.two weeks of intervention

Countries

China

Contacts

CONTACTJie Zhang
zhangjie9496@bucm.edu.cn+86 15652385971

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026