CClinicalTrials.gg
Status unknownNCT03193502Updated Oct 13, 2017

Efficacy and Safety of Rivaroxaban in the Management of Acute Non-neoplastic PVT Compensated Cirrhosis

A Phase 3 interventional study of rivaroxaban in Portal Vein Thrombosis, sponsored by Sherief Abd-Elsalam. Status unknown at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2017-10-13.

Sponsored by Sherief Abd-Elsalam · Phase 3, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Oct 2017), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 3 years 1 month after the study started (first participant enrolled May 2014, registered Jun 2017).
Phase
Phase 3
Study type
Interventional
Enrollment
40
Allocation
Not applicable
Sex
All
01

Study summary

-Rivaroxaban is factor Xa inhibitor

Read the detailed description

PVT is a common complication of liver cirrhosis

02

Conditions studied

  • Portal Vein Thrombosis
03

In context

Thrombosis

1,506 studies on the registry are indexed under Thrombosis; 238 are open to participants now.

This study's planned enrollment of 40 is below the median of 106 across 849 interventional studies indexed under Thrombosis.

Browse Thrombosis studies →

Lead sponsor

Sherief Abd-Elsalam is the lead sponsor of 50 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Acute PVT

Exclusion criteria

Exclusion Criteria:

  • Malignant PVT
  • Bleeding disorders
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Portal Vein thrombosis

    rivaroxaban

    Drug: rivaroxaban

Interventions

  • Drugrivaroxaban

    rivaroxaban

    Also known as: xarelto

06

What researchers measure

Primary outcomes

  1. Number of patients with recanalized portal vein

    recanalization of portal vein

    Time frame: 6 months

07

Study locations

1 of 1 sites recruiting
  • Tropical medicine dept.-Tanta university hospital
    Cairo, Egypt
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 13, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03193502
Lead sponsor
Sherief Abd-Elsalam
Responsible party
Sherief Abd-Elsalam (Consultant, Tanta University) — Sponsor-investigator
First posted
Jun 20, 2017
Start date
May 1, 2014
Primary completion
Jul 2020 (estimated)
Completion
Dec 2020 (estimated)
Last update
Oct 13, 2017

Study contacts

Sherief Abd-Elsalam, consultant
Contact
Sheriefabdelsalam@yahoo.com
00201095159522
Amr Hanafy, Professor
principal investigator · Hepatology unit - Zagazig University
Mohamed Basha, Consultant
study director · Radiology Dept - Zagazig University
Sherief Abd-elsalam, consultant
study chair · Hepatology - Gastroenterology - Tanta University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2017. You cannot join it, but the record below documents what was studied.

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