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Not yet recruitingNCT07834918Updated Sep 22, 2026

Pulmonary Hypertension and RV Dysfunction in Myeloproliferative Neoplasms

An observational study in Myeloproliferative Neoplasm, Right Ventricular Dysfunction and Pulmonary Hypertension, sponsored by Assiut University. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-22.

Sponsored by Assiut University · Observational

Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
145
Ages
18 Years and older
Sex
All
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Study summary

This cross-sectional study aims to determine the prevalence of pulmonary hypertension and right ventricular dysfunction in patients with myeloproliferative neoplasms and to identify associated clinical and hematologic factors.

Read the detailed description

Myeloproliferative neoplasms (MPNs) are associated with an increased risk of pulmonary hypertension and right ventricular dysfunction. This observational study will include adults with confirmed polycythemia vera, essential thrombocythemia, or primary myelofibrosis.

All participants will undergo clinical assessment, laboratory evaluation, and echocardiography to assess pulmonary artery systolic pressure and right ventricular systolic function (TAPSE, FAC, and tissue Doppler S').

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Conditions studied

  • Myeloproliferative Neoplasm
  • Right Ventricular Dysfunction
  • Pulmonary Hypertension

Keywords

  • Assiut
  • Echocardiography
  • Right ventricular dysfunction
  • Myeloproliferative neoplasm
  • Pulmonary hypertension
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In context

Myeloproliferative Disorders

667 studies on the registry are indexed under Myeloproliferative Disorders; 110 are open to participants now.

This study's planned enrollment of 145 is close to the median of 150 across 115 observational studies indexed under Myeloproliferative Disorders.

Browse Myeloproliferative Disorders studies →

Lead sponsor

Assiut University is the lead sponsor of 5,078 studies on the registry; 2,178 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult patients with confirmed myeloproliferative neoplasms (polycythemia vera, essential thrombocythemia, or primary myelofibrosis) attending the Hematology Unit and Critical Care Department at Assiut University Hospital.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • - Age 18 years or older
  • Confirmed diagnosis of myeloproliferative neoplasm (polycythemia vera, essential thrombocythemia, or primary myelofibrosis)
  • Stable clinical condition
  • Written

Exclusion criteria

Exclusion Criteria:

  • - Significant left-sided valvular heart disease
  • Congenital heart disease
  • or interstitial lung disease causing pulmonary hypertension
  • Poor echocardiographic window
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

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Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
145 participants (estimated)
Patient registry
No

Groups and cohorts

  • Single cohort: Patients with myeloproliferative neoplasms

    Adult patients with myeloproliferative neoplasms who will undergo clinical, laboratory, and echocardiographic assessment for pulmonary hypertension and right ventricular dysfunction.

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What researchers measure

Primary outcomes

  1. Prevalence of Pulmonary Hypertension in MPN Patients

    PASP measured by echocardiography using TR velocity. Pulmonary hypertension defined as PASP greater than 35 mmHg or TR velocity greater than 2.8 m/s. Prevalence will be calculated.

    Time frame: Baseline

Secondary outcomes

  1. Prevalence of right ventricular dysfunction

    Proportion of patients with right ventricular dysfunction defined by TAPSE \<17 mm, RV fractional area change \<35%, or tissue Doppler S' \<9.5 cm/s

    Time frame: Baseline

  2. Pulmonary artery systolic pressure

    Mean estimated pulmonary artery systolic pressure (mmHg) measured by echocardiography

    Time frame: Baseline

  3. Tricuspid annular plane systolic excursion (TAPSE)

    Mean TAPSE value (mm) measured by echocardiography.

    Time frame: Baseline

  4. Right ventricular fractional area change

    Mean right ventricular fractional area change (%) measured by echocardiography.

    Time frame: Baseline

07

Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Sep 2026; primary completion for Sep 2027, 12 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 17, 2026
First posted
Sep 22, 2026
StartEst.
Sep 20, 2026
Primary completionEst.
Sep 20, 2027
CompletionEst.
Mar 10, 2028
Last update
Sep 22, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07834918
Lead sponsor
Assiut University
Responsible party
Esraa medhat Ahmed (Resident Physician, Assiut University) — Principal investigator
First posted
Sep 22, 2026
Start date
Sep 20, 2026 (estimated)
Primary completion
Sep 20, 2027 (estimated)
Completion
Mar 10, 2028 (estimated)
Last update
Sep 22, 2026

Study contacts

Esraa M Ahmed, Resident
Contact
esraamedhat449@gmail.com
+20 10 99071931
Refaat f abdel all, prof
study chair · Critical care unit Internal Medicine Department, Assiut University Hospitals

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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