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Pulmonary HypertensionMIRROR-PAHNCT07667673

Multimodality RV Phenotyping for Risk Stratification and Short-Term Outcomes in Group 1 PAH

An observational study of Pulmonary Hypertension and Pulmonary Arterial Hypertension, run by Istanbul University - Cerrahpasa at 1 site in Turkey (Türkiye).

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The MIRROR-PAH is a single-center, prospective, observational cohort study evaluating the incremental value of multimodality imaging-derived right ventricular characteristics for risk stratification in patients with Group 1 pulmonary arterial hypertension (PAH). Read more about this study

Who is it for?
Ages 18 years and older
How many people
50 participants
Where
1 siteTurkey (Türkiye)
Study dates
11 May 2026to May 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients with established Group 1 pulmonary arterial hypertension (PAH) undergoing routine follow-up at a specialized pulmonary hypertension center. Eligible participants will have available right heart catheterization (RHC), transthoracic echocardiography, and cardiac magnetic resonance (CMR) imaging data and will undergo prospective clinical and echocardiographic follow-up for 6 months.

Who may be able to join

  • Adults aged 18 years or older
  • Diagnosis of Group 1 pulmonary arterial hypertension (PAH) according to ESC/ERS guidelines
  • Followed at the study center with a diagnosis of PAH
  • Availability of right heart catheterization (RHC) and cardiac magnetic resonance (CMR) imaging data obtained within a clinically relevant time interval
  • Availability of analyzable clinical, imaging, and hemodynamic data
  • Willingness to participate in the study and provision of written informed consent

Who cannot join

  • Age younger than 18 years
  • Pulmonary hypertension groups other than Group 1 PAH (Groups 2-5 PH)
  • Absence of either right heart catheterization or cardiac magnetic resonance imaging data within a clinically relevant time interval
  • Incomplete clinical or imaging data preventing analysis
  • Unavailable follow-up data

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Istanbul University Cerrahpasa Institute of Cardiology

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: Multimodality Imaging-Based Right Ventricular Phenotyping for Risk Stratification and Short-Term Outcomes in Group 1 Pulmonary Arterial Hypertension: The MIRROR-PAH Study

The MIRROR-PAH is a single-center, prospective, observational cohort study evaluating the incremental value of multimodality imaging-derived right ventricular characteristics for risk stratification in patients with Group 1 pulmonary arterial hypertension (PAH). The study aims to determine whether incorporation of echocardiographic and cardiac magnetic resonance (CMR)-derived right ventricular parameters into established non-invasive risk assessment models results in risk reclassification and improves identification of patients at risk for short-term clinical worsening.

Adult patients with established Group 1 PAH undergoing routine follow-up and with available right heart catheterization (RHC) and CMR data will be consecutively enrolled. Clinical, laboratory, echocardiographic, and follow-up data will be prospectively collected over a 6-month period. Associations between multimodality imaging findings, invasive hemodynamic measurements, risk classification, and short-term clinical outcomes will be evaluated.

Read the detailed description

Pulmonary arterial hypertension (PAH) is a progressive disease characterized by pulmonary vascular remodeling, increased pulmonary vascular resistance, and progressive right ventricular (RV) pressure overload. Despite substantial advances in targeted therapies, morbidity and mortality remain high, and patient prognosis is largely determined by the ability of the right ventricle to adapt to the increased afterload imposed by the pulmonary circulation.

Current clinical practice guidelines recommend periodic risk assessment to guide treatment decisions and monitor disease progression. Contemporary non-invasive risk stratification models incorporate clinical, functional, and biochemical parameters, including World Health Organization (WHO) functional class, exercise capacity, and natriuretic peptide levels. Although cardiac imaging provides important information regarding right ventricular structure and function and is widely used during the evaluation and follow-up of patients with PAH, imaging parameters are not routinely incorporated into simplified follow-up risk assessment models. Consequently, a considerable proportion of patients remain classified within intermediate-risk categories, representing a heterogeneous population with variable clinical trajectories and therapeutic needs.

Multimodality cardiac imaging provides comprehensive assessment of right ventricular structure, function, and remodeling. Echocardiography remains the cornerstone imaging modality for routine evaluation and longitudinal follow-up of PAH patients, while cardiac magnetic resonance (CMR) offers highly accurate and reproducible quantification of right ventricular volumes and function. Several imaging-derived parameters have been associated with disease severity and adverse outcomes in PAH. In addition, invasive hemodynamic assessment obtained by right heart catheterization (RHC) provides important prognostic information regarding pulmonary vascular disease and right ventricular adaptation. The integration of imaging and hemodynamic information may therefore provide incremental value beyond conventional non-invasive risk assessment strategies.

The MIRROR-PAH Study (Multimodality Imaging-Based Right Ventricular Phenotyping for Risk Stratification and Short-Term Outcomes in Group 1 Pulmonary Arterial Hypertension) is a single-center, prospective, observational cohort study designed to evaluate the relationship between multimodality imaging-derived right ventricular characteristics, invasive hemodynamic measurements, established risk assessment models, and short-term clinical outcomes in patients with Group 1 PAH.

Adult patients with established Group 1 PAH who are undergoing routine follow-up and have available RHC and CMR examinations will be consecutively enrolled. Baseline clinical, laboratory, echocardiographic, hemodynamic, and CMR data will be collected. Follow-up clinical assessment and transthoracic echocardiography will be performed at 6 months.

The primary objective of the study is to determine whether incorporation of multimodality imaging-derived right ventricular (RV) characteristics into established non-invasive PAH risk assessment models results in risk reclassification at baseline and at 6-month follow-up.

Secondary objectives are to:

  • Evaluate the predictive value of imaging-augmented risk reclassification for composite clinical worsening during follow-up;
  • Assess the incidence of composite clinical worsening, defined as PAH treatment escalation, PAH-related hospitalization, worsening WHO functional class, decline in 6-minute walk distance, or death;
  • Identify multimodality imaging-derived RV characteristics associated with an increased risk of short-term clinical worsening;
  • Evaluate the relationship between multimodality imaging-derived RV characteristics and invasive hemodynamic measurements obtained by right heart catheterization (RHC);
  • Identify multimodality imaging-derived RV characteristics associated with high-risk classification according to established PAH risk stratification models;
  • Evaluate changes in echocardiographic RV characteristics between baseline and 6-month follow-up;
  • Assess the incremental prognostic value of multimodality imaging-derived RV characteristics beyond established non-invasive PAH risk assessment models for predicting clinical worsening.

The study is based on the hypothesis that multimodality assessment of right ventricular structure and function provides clinically relevant information beyond conventional non-invasive risk stratification models and may improve identification of patients at increased risk of disease progression and short-term adverse outcomes. By integrating echocardiographic, CMR, and invasive hemodynamic information, the MIRROR-PAH Study aims to explore the potential role of imaging-enhanced risk assessment in refining prognostic evaluation and supporting clinical decision-making during follow-up of patients with PAH.

Keywords
pulmonary arterial hypertension, transthoracic echocardiography, cardiac magnetic resonance imaging, right heart catheterization, risk stratification
Medical subject headings
Hypertension, Pulmonary, Pulmonary Arterial Hypertension

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07667673
Study groupRoleWhat they receive
Patients with Group 1 Pulmonary Arterial HypertensionParticipants are adult patients with established Group 1 pulmonary arterial hypertension (PAH) undergoing follow-up at a specialized pulmonary hypertension center.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Risk reclassification rate after incorporation of multimodality imaging-derived RV characteristics into established non-invasive PAH risk models

    The proportion of patients undergoing risk reclassification after incorporation of multimodality imaging-derived right ventricular (RV) characteristics obtained from echocardiography and cardiac magnetic resonance imaging into established non-invasive PAH risk assessment models will be evaluated. Changes in risk category assignment compared with conventional non-invasive risk stratification will be assessed.

    Measured: Baseline and 6-month follow-up

Secondary outcomes (6)
  1. Number of Participants Experiencing Composite Clinical Worsening

    Composite clinical worsening is defined as the occurrence of at least one of the following events during the 6-month follow-up period: pulmonary arterial hypertension (PAH) treatment escalation, PAH-related hospitalization, worsening World Health Organization (WHO) functional class, decline in 6-minute walk distance, or death.

    Measured: 6 months

  2. Change in Predictive Performance for Composite Clinical Worsening After Addition of RV Imaging Characteristics to Conventional PAH Risk Classification

    The predictive performance of conventional three-strata pulmonary arterial hypertension risk classification for 6-month composite clinical worsening will be compared with the predictive performance of an imaging-augmented risk classification incorporating predefined right ventricular imaging characteristics. Predictive performance will be assessed using the area under the receiver operating characteristic curve.

    Measured: 6 months

  3. RV imaging characteristics associated with clinical worsening

    Multimodality imaging-derived RV characteristics associated with an increased risk of composite clinical worsening will be identified.

    Measured: 6 months

  4. Agreement Between Cardiovascular Magnetic Resonance-Derived Stroke Volume Index and Right Heart Catheterization-Derived Stroke Volume Index

    Agreement between stroke volume index (mL/m²) measured by cardiovascular magnetic resonance imaging using ventricular volumetric analysis and stroke volume index (mL/m²) calculated from cardiac output obtained during right heart catheterization will be assessed at baseline using Bland-Altman analysis. The mean difference in stroke volume index (mL/m²) between the two methods will be reported.

    Measured: Baseline

  5. RV imaging characteristics associated with high-risk status

    Multimodality imaging-derived RV characteristics associated with high-risk classification according to established PAH risk assessment models will be identified.

    Measured: Baseline and 6-month follow-up

  6. Change in Right Ventricular Free-Wall Longitudinal Strain From Baseline to 6 Months

    Change in right ventricular free-wall longitudinal strain (%) measured by two-dimensional speckle-tracking echocardiography will be assessed between baseline and the 6-month follow-up. The mean change in right ventricular free-wall longitudinal strain (%) from baseline to 6 months will be reported.

    Measured: Baseline to 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Jun 2026
  2. Study start11 May 2026
  3. Primary completionFeb 2027 (estimated)
  4. Study completionMay 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07667673
Sponsor's protocol ID
2026/171
Acronym
MIRROR-PAH
Status last verified
Jun 2026
First submitted
6 Jun 2026
Last updated
18 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Individual participant data (IPD) sharing plans have not yet been determined. Any future data sharing will be subject to institutional policies, ethical considerations, participant confidentiality requirements, and applicable regulations.

Publications

  • Lewis RA, Johns CS, Cogliano M, Capener D, Tubman E, Elliot CA, Charalampopoulos A, Sabroe I, Thompson AAR, Billings CG, Hamilton N, Baster K, Laud PJ, Hickey PM, Middleton J, Armstrong IJ, Hurdman JA, Lawrie A, Rothman AMK, Wild JM, Condliffe R, Swift AJ, Kiely DG. Identification of Cardiac Magnetic Resonance Imaging Thresholds for Risk Stratification in Pulmonary Arterial Hypertension. Am J Respir Crit Care Med. 2020 Feb 15;201(4):458-468. doi: 10.1164/rccm.201909-1771OC.

    PubMed 31647310
  • Dardi F, Boucly A, Benza R, Frantz R, Mercurio V, Olschewski H, Radegran G, Rubin LJ, Hoeper MM. Risk stratification and treatment goals in pulmonary arterial hypertension. Eur Respir J. 2024 Oct 31;64(4):2401323. doi: 10.1183/13993003.01323-2024. Print 2024 Oct.

    PubMed 39209472
  • Humbert M, Kovacs G, Hoeper MM, Badagliacca R, Berger RMF, Brida M, Carlsen J, Coats AJS, Escribano-Subias P, Ferrari P, Ferreira DS, Ghofrani HA, Giannakoulas G, Kiely DG, Mayer E, Meszaros G, Nagavci B, Olsson KM, Pepke-Zaba J, Quint JK, Radegran G, Simonneau G, Sitbon O, Tonia T, Toshner M, Vachiery JL, Vonk Noordegraaf A, Delcroix M, Rosenkranz S; ESC/ERS Scientific Document Group. 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension. Eur Respir J. 2023 Jan 6;61(1):2200879. doi: 10.1183/13993003.00879-2022. Print 2023 Jan. No abstract available.

    PubMed 36028254

Questions about this trial

What is this clinical trial studying?

An observational study of Pulmonary Hypertension and Pulmonary Arterial Hypertension, run by Istanbul University - Cerrahpasa at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 18 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Risk reclassification rate after incorporation of multimodality imaging-derived RV characteristics into established non-invasive PAH risk models (time frame: Baseline and 6-month follow-up). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07667673, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Sep 2026.

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