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RecruitingNot a traditional drug phaseobservationalRules rewrite

Not a traditional drug phase: Endovascular Intervention for Portal Hypertension-Related Gastrointestinal Bleeding for Cirrhosis

Portal hypertension-related gastrointestinal bleeding (GIB), especially gastric variceal bleeding, is a critical complication of liver cirrhosis that is associated with high rebleeding and mortality rates. While endovascular interventions such as transjugular intrahepatic portosystemic shunt (TIPS) and retrograde/antegrade transvenous obliteration (RTO/ATO) represent major advances, real-world clinical data and localized prognostic models for patients undergoing these treatments are extremely sparse in Vietnam.

Official registry: https://clinicaltrials.gov/study/NCT07918378 · University Medical Center Ho Chi Minh City (UMC) · enrollment listed as 167

What this phase means

This is an observational study. You are not assigned a new experimental drug. Researchers measure what already happens in your care or in daily life.

Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

What the registry says happens

This listing is observational (StudyType). The registry does not assign a new experimental drug as the study intervention.

They plan to enroll about 167 people at Ho Chi Minh City. Taking part typically means a procedure as part of the study plus check-ins.

Official title (unrewritten)

Treatment Outcomes and Predictors After Endovascular Intervention for Portal Hypertension-Related Gastrointestinal Bleeding in Patients With Cirrhosis at University Medical Center Ho Chi Minh City

Interventions: Endovascular Intervention for Portal Hypertension-Related Gastrointestinal Bleeding

Primary outcome (registry wording): Number of Participants With a Composite Adverse Clinical Outcome After Endovascular Intervention

Who it is for (from inclusion criteria)

  • Ages 18 Years to any
  • Patient is aged 18 years or older on the day of admission
  • Confirmed diagnosis of liver cirrhosis by attending clinicians based on clinical findings, laboratory tests, imaging studies (ultrasound, CT, MRI, elastography), or liver histology if available
  • Diagnosis of acute portal hypertension-related gastrointestinal bleeding requiring treatment with at least one endovascular intervention technique (TIPS, PARTO, CARTO, ATO, or combined techniques)

Public study contact (from the registry)

Assoc. Professor. Thong Duy Vo, M.D. Ph.D.

+84 932039888

thong.vd@umc.edu.vn

Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.

Sites listed on ClinicalTrials.gov

1 listed

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FAQ about this NCT record

Is NCT07918378 still recruiting?

The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.

What phase is NCT07918378?

Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

Can PlainTrials tell me if I qualify for NCT07918378?

No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.

How to read a ClinicalTrials.gov record · Questions to ask the coordinator · Glossary