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Life-2023-02 Esophagogastric Variceal Bleeding

Zhejiang University logo

Zhejiang University

Status

Enrolling

Conditions

Acute Esophageal Variceal Hemorrhage

Treatments

Drug: Growth Inhibitor

Study type

Interventional

Funder types

Other

Identifiers

NCT06011980
2023-0407

Details and patient eligibility

About

Study on the efficacy of the growth inhibitors after endoscopic treatment of acute esophagogastric variceal bleeding

Full description

Participants with acute esophagogastric variceal bleeding in 5 days and under stable status will be included in this study. All the patients will take CTP test to confirm the blood flow status of the portal vein before endoscopic treatment. After that they will be randomly divided into two groups: A. accept growth inhibitors after the endoscopic treatment for 5 days; B. no growth inhibitor will be applied after the treatment.

Enrollment

33 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • acute esophagogastric bleeding with hepatic cirhosis;
  • stable status (no active bleeding)

Exclusion criteria

  • endoscopic test limitation;
  • previous acute esophagogastric bleeding treatment history;
  • ICU;
  • pregnant;
  • Immunity disabled;

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

33 participants in 2 patient groups

Group A
Experimental group
Description:
Participants in this group will take growth inhibitors for 5 days after endoscopic treatment.
Treatment:
Drug: Growth Inhibitor
Group B
No Intervention group
Description:
Participants in this group will not take growth inhibitor treatment after endoscopic treatment.

Trial contacts and locations

1

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Central trial contact

WEI WEI

Data sourced from clinicaltrials.gov

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