Registry of Patients With chrOnic thromboemboLic Pulmonary hypErTension
POLET
Registry of Patients With Chronic Thromboembolic Pulmonary Hypertension in Russia: Determinants of Long-term Outcomes in Real Clinical Practice
1 other identifier
observational
500
1 country
1
Brief Summary
The goal of this observational study is to gather information on background, medical history, symptoms and physical condition, treatment options of people with chronic thromboembolic pulmonary hypertension in real clinical practice in Russia. The main question it aims to answer is: Which factors most influence the prognosis of participants?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2025
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2025
CompletedFirst Submitted
Initial submission to the registry
November 19, 2025
CompletedFirst Posted
Study publicly available on registry
November 28, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2035
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 1, 2035
December 12, 2025
December 1, 2025
10 years
November 19, 2025
December 4, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
All-cause mortality
Up to 5 years
Secondary Outcomes (3)
All-cause mortality
Up to 10 years
Change in distance in 6-minute walk test
1 year
Change in mPAP
1 year
Interventions
A surgical procedure to remove chronic blood clots from the pulmonary arteries
A minimally invasive procedure used to treat chronic thromboembolic pulmonary hypertension by dilatating narrowed pulmonary arteries and improving blood flow to the lungs
Medical treatment with any PH-specific drugs
Eligibility Criteria
operable CTEPH, non-operable CTEPH
You may qualify if:
- Presence of a confirmed diagnosis of CTEPH
You may not qualify if:
- Presence of pulmonary hypertension of a different etiology than CTEPH
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Irina E. Chazovalead
Study Sites (1)
National Medical Research Center of Cardiology after academician E.I. Chazov
Moscow, Russia
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- OTHER
- Target Duration
- 10 Years
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- D. Sci. (Med.), Acad. RAS, Prof., Deputy Director General for Scientific and Expert Work, FSBI NATIONAL MEDICAL RESEARCH CENTRE OF CARDIOLOGY NAMED AFTER ACADEMICIAN E.I.CHAZOV of the Ministry of Health of the Russian Federation
Study Record Dates
First Submitted
November 19, 2025
First Posted
November 28, 2025
Study Start
May 1, 2025
Primary Completion (Estimated)
May 1, 2035
Study Completion (Estimated)
May 1, 2035
Last Updated
December 12, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share