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Cavernous Transformation of Portal Vein: Etiology, Diagnosis, Management and Prognosis

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Sun Yat-sen University

Status

Unknown

Conditions

Portal Vein, Cavernous Transformation Of

Treatments

Drug: Montelukast

Study type

Observational

Funder types

Other

Identifiers

NCT02505113
CTPVDORNO3HSYSU

Details and patient eligibility

About

To observe the etiology, diagnosis, management and prognosis of cavernous transformation of portal vein.

Full description

To observe the etiology, diagnosis, management and prognosis of cavernous transformation of portal vein.

We perform Montelukast (10mg, q.d., p.o.) fot the treatment of symptomatic cavernous transformation of portal vein and to observe the efficacy such as the decrease of the volume of ascites and hydrothorax.

Enrollment

150 estimated patients

Sex

All

Ages

1 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients with CTPV.

Exclusion criteria

  • Patients with known severe dysfunction of heart, lung, brain, kidney and other vital organs.

Trial design

150 participants in 2 patient groups

CTPV without Montelukast
Description:
Patients with CTPV do not receive the treatment of Montelukast.
CTPV treated with Montelukast
Description:
Patients with CTPV treated with Montelukast (10mg, q.d., p.o.).
Treatment:
Drug: Montelukast

Trial contacts and locations

1

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Central trial contact

Zaibo Jiang, MD

Data sourced from clinicaltrials.gov

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