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RecruitingNCT07254078POLETUpdated Dec 12, 2025

Registry of Patients With chrOnic thromboemboLic Pulmonary hypErTension

An observational study in Chronic Thromboembolic Pulmonary Hypertension, sponsored by Irina E. Chazova. Recruiting at 1 site in Russia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-12-12.

Sponsored by Irina E. Chazova · Observational

From the registry’s dates

  • Started May 2025; still recruiting 1 year 5 months later.
Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
500
Ages
18 Years and older
Sex
All
01

Study 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?

Read the detailed description

Data from international CTEPH registries indicate variable utilization rates of available treatment options. Considering the presence of national specificities in the management of CTEPH patients, coupled with the relatively low prevalence of the disease, which poses challenges for data accumulation and research, new registry POLET (Registry of Patients with chrOnic thombomboLic pumonary hypErTension) is established to investigate CTEPH patients in real-world clinical practice.

Registry Aim:

To investigate the prognosis of patients with chronic thromboembolic pulmonary hypertension based on demographic, anamnestic, clinical characteristics, and treatment regimens.

Registry Objectives:

To describe the key demographic, anamnestic, and clinical characteristics of CTEPH patients in Russia.

To identify factors influencing the frequency of hospitalizations due to clinical deterioration in CTEPH patients.

To determine the impact of anamnestic data and treatment regimens on patient prognosis (time to clinical deterioration/death).

To determine the impact of demographic and clinical characteristics on patient survival and prognosis (time to clinical deterioration/death).

Currently, preliminary retrospective data have been collected on 300 CTEPH patients, each with 1 to 15 hospitalizations at the National Medical Research Center of Cardiology named after Academician E.I. Chazov of the Ministry of Health of Russia from 2012-2024, and who are eligible for inclusion in the registry. 200 patients will be enrolled prospectively.

The following data to be extracted from electronic medical records:

Medical History Data; Clinical Characteristics and Results of Investigations and Treatments During Each Patient Hospitalization; Operability Assessment Results; PAH-Specific Therapy, Anticoagulant Therapy, Supportive Therapy: Therapy Adjustment, Doses, Presence of Side Effects; Details of Pulmonary endarterectomy; Details of BPA performed; Patient outcomes including survival. Statistical data processing will be performed using RStudio and the R programming language. Missing data will be handled with imputation approach.

02

Conditions studied

  • Chronic Thromboembolic Pulmonary Hypertension

Keywords

  • CTEPH
  • registry
  • PEA
  • BPA
  • PAH-specific therapy
  • survival
03

In context

Lead sponsor

This is the only study on the registry with Irina E. Chazova as lead sponsor.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

operable CTEPH, non-operable CTEPH

Inclusion criteria

  • Presence of a confirmed diagnosis of CTEPH

Exclusion criteria

Exclusion Criteria:

  • Presence of pulmonary hypertension of a different etiology than CTEPH
05

Study design

Observational model
Cohort
Time perspective
Other
Enrollment
500 participants (estimated)
Target follow-up
10 Years
Patient registry
Yes

Interventions

  • ProcedurePulmonary endarterectomy

    A surgical procedure to remove chronic blood clots from the pulmonary arteries

    Also known as: PEA, PTE, Pulmonary thromboendarterectomy

  • ProcedureBalloon pulmonary angioplasty

    A minimally invasive procedure used to treat chronic thromboembolic pulmonary hypertension by dilatating narrowed pulmonary arteries and improving blood flow to the lungs

    Also known as: BPA

  • DrugPulmonary hypertension-specific therapy

    Medical treatment with any PH-specific drugs

    Also known as: PH-specific therapy, PH-Targeted Medical Therapy

06

What researchers measure

Primary outcomes

  1. All-cause mortality

    Time frame: Up to 5 years

Secondary outcomes

  1. All-cause mortality

    Time frame: Up to 10 years

  2. Change in distance in 6-minute walk test

    Time frame: 1 year

  3. Change in mPAP

    mPAP assesed during right heart catheterization

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • National Medical Research Center of Cardiology after academician E.I. Chazov
    Moscow, Russia
    • Galina V Schelkova · Contact · GVShchelkova@Cardio.ru · +74954146270
    • Irina E Chazova, D. Sci. (Med.) · Principal investigator
    • Nikolay M Danilov, D. Sci. (Med.) · Principal investigator
    • Galina V Schelkova, PhD · Sub investigator
    • Sergey Y Yarovoy, PhD · Sub investigator
    • Ekaterina O Dinevich · Sub investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

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 Dec 12, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07254078
Lead sponsor
Irina E. Chazova
Responsible party
Irina E. Chazova (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, National Medical Research Center for Cardiology, Ministry of Health of Russian Federation) — Sponsor-investigator
First posted
Nov 28, 2025
Start date
May 1, 2025
Primary completion
May 1, 2035 (estimated)
Completion
May 1, 2035 (estimated)
Last update
Dec 12, 2025

Oversight

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

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No contact was published for this record. The registry link below has the sponsor’s details.

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