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A Real World Study of the Treatment of Gastric Adenocarcinoma With Huachansu

C

China Resources Sanjiu Medical & Pharmaceutical

Status

Unknown

Conditions

Gastric Adenocarcinoma

Study type

Observational

Funder types

Industry

Identifiers

NCT05249244
ICM-HCS-CR01

Details and patient eligibility

About

To evaluate the efficacy and safety of huachansu oral preparation in the treatment of inoperable locally advanced or advanced metastatic gastric adenocarcinoma, including gastric esophageal adenocarcinoma.

Full description

In this multicenter, controlled, retrospective, real-world study, the original medical records of participants diagnosed with inoperable locally advanced or advanced metastatic gastric adenocarcinoma (including gastric esophageal junction adenocarcinoma) receive treatment in research centers from January 1, 2014 to December 31, 2019 were collected. To evaluate the efficacy and safety of oral huachansu in the systematic treatment of locally advanced or advanced metastatic gastric adenocarcinoma.

Enrollment

1,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

Only patients who meet all the following criteria are included in the study:

  1. Diagnosed with gastric adenocarcinoma (including gastric esophageal junction adenocarcinoma) by histopathology or cytology at the enrolled centers From January 1, 2014 to December 31, 2019.
  2. Stage of disease (clinical or pathological stage) is locally advanced or advanced (stage IIIB-IV) .
  3. The doctor judged that the tumor tissue was unresectable.
  4. At least two medical records.
  5. At least one huachansu oral preparation (tablet, capsule) was used during treatment (observation group only) .

Exclusion criteria

Patients who meet any of the following criteria are not allowed to enter the test:

  1. Lack of clinical data related to important research indicators (survival).
  2. Refusal to cooperate with follow-up.

Trial design

1,000 participants in 2 patient groups

observation group
Description:
huachansu oral preparation (tablet, capsule) was used.
control group
Description:
huachansu was not used.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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