Trial · NCT02335580
Effect of Portal Vein Thrombosis on the Prognosis of Liver Cirrhosis
NCT02335580, Completed, General Hospital of Shenyang Military Region
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Portal Vein Thrombosis on the Prognosis of Liver Cirrhosis. Trials, record NCT02335580. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02335580
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Portal Vein Thrombosis on the Prognosis of Liver Cirrhosis
- NCT number
- NCT02335580
- Status
- Completed
- Enrollment
- 475 participants, actual
- Lead sponsor
- General Hospital of Shenyang Military Region
- Conditions
- Liver Cirrhosis, Portal Vein, Venous Thrombosis, Varicose Veins, Hemorrhage
- Interventions
- Somatostatin and its analogs, Endoscopic sclerotherapy, endoscopic variceal ligation, endoscopic tissue glue injection
- First posted
- 2015-01-12
- Last updated
- 2023-02-24
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Overall survival | 6-24 months | |
| Primary | First bleeding | 0-24 months | As for the patients without any prior history of bleeding but with high-risk varices, the first bleeding was observed. |
| Primary | Recurrent bleeding | 0-24 months | As for the patients with a prior history of bleeding, the recurrent bleeding was observed. |
| Primary | Treatment failure rate of acute variceal bleeding | 5 days | As for the patients with acute variceal bleeding, the 5-day treatment failure of acute bleeding was observed. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers7
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02335580
GET https://conductscience.org/api/trials/v1/NCT02335580/registered