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Delayed Diagnosis Pulmonary HypertensionNCT07810881

Diagnostic Delay in PHTN

An observational study of Delayed Diagnosis Pulmonary Hypertension, run by Assiut University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Pulmonary hypertension (PH) is a progressive cardiopulmonary condition that may remain undiagnosed for a prolonged period because its initial symptoms are often nonspecific. This study aims to assess the relationship between diagnostic delay and disease severity at the time of initial presentation among adult patients… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Delayed Diagnosis Pulmonary Hypertension
How many people
80 participants
Where
No sites listed yet
Study dates
1 Sep 2026to 1 Dec 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 (aged 18 years or older) with pulmonary hypertension who present to the Pulmonary Hypertension Unit/Cardiology Department at Assiut University Heart Hospital during the study period. Participants will include patients with pulmonary hypertension confirmed by right heart catheterization when available, or patients with high echocardiographic probability or a clinician diagnosis of pulmonary hypertension when right heart catheterization is not available.

Who may be able to join

  • 1. Age 18 years or older
  • 2. Patients with pre-capillary pulmonary hypertension, Group 1 PAH, Group 3 PH associated with lung disease/hypoxia, Group 4 chronic thromboembolic pulmonary hypertension (CTEPH) or other pulmonary artery obstructions, and Group 5 PH with unclear or multifactorial mechanisms.
  • 3. Diagnosis of pulmonary hypertension based on RHC when available, or high echocardiographic probability/clinician diagnosis of PH when RHC is not available.
  • 4. Availability of baseline clinical assessment at or near the time of diagnosis or first PH-unit presentation.
  • 5. Ability to provide an approximate date or month/year of first PH-related symptom.
  • 6. Willingness to participate and provide informed consent.

Who cannot join

  • 1. Inability to provide reliable information about symptom onset and no alternative documentation in the medical record.
  • 2. Incomplete baseline data preventing classification of disease severity. 3. Post-capillary pulmonary hypertension due to left heart disease (Group 2 PH).
  • 4. Acute pulmonary embolism as the sole acute cause of transient pulmonary pressure elevation at presentation.
  • 5. Severe acute illness, cognitive impairment, or communication barrier preventing questionnaire completion.
  • 6. Refusal to participate. 7. Optional exclusion according to committee preference: patients with isolated post-capillary PH due to left heart disease may be excluded if the aim is to focus on PAH/pre-capillary PH.

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Abanoub Felemon contact

+201283656965

Bebomessi30@gmail.com

Mahmoud Abdelsabour, Professor contact

About this study

Official title: Diagnostic Delay in Pulmonary Hypertension: Determinants and Impact on Disease Severity at Initial Presentation

Pulmonary hypertension (PH) is a progressive cardiopulmonary condition that may remain undiagnosed for a prolonged period because its initial symptoms are often nonspecific. This study aims to assess the relationship between diagnostic delay and disease severity at the time of initial presentation among adult patients with pulmonary hypertension at Assiut University Heart Hospital. The study will use an observational cross-sectional analytical design with retrospective review of available medical records and prospective data collection. Eligible patients will be consecutively recruited. Data will include demographic and clinical characteristics, duration of symptoms before diagnosis, previous medical consultations and diagnoses, WHO functional class, six-minute walk distance, echocardiographic findings, laboratory investigations, and available right heart catheterization data. The primary outcome is advanced disease at presentation, defined as WHO functional class III-IV. The study will also assess clinical, echocardiographic, functional, and hemodynamic markers of disease severity and potential factors associated with diagnostic delay.

Read the detailed description

Pulmonary hypertension (PH) is a complex cardiopulmonary syndrome associated with progressive pulmonary vascular disease and right ventricular overload. Its early clinical manifestations, including exertional dyspnea, fatigue, reduced exercise tolerance, chest discomfort, palpitations, presyncope, syncope, and peripheral edema, are often nonspecific and may overlap with common cardiac, respiratory, hematological, and other conditions. This may contribute to delayed recognition and referral for specialist assessment.

The present study aims to assess the relationship between the duration of diagnostic delay and disease severity at the time of initial presentation among adult patients with pulmonary hypertension attending the Pulmonary Hypertension Unit at Assiut University Heart Hospital. The study will also identify potential patient- and healthcare-related factors associated with delayed diagnosis.

This will be an observational cross-sectional analytical study with retrospective chart review and prospective data collection. Consecutive sampling will be used. All eligible adult patients with pulmonary hypertension fulfilling the predefined inclusion criteria will be recruited until the required sample size is reached. Patients identified from previously available medical records may be included when the required clinical and investigation data are available and the patient fulfills the eligibility criteria. Relevant prospective data will be collected during the study period.

Eligible participants will be adults aged 18 years or older with pulmonary hypertension diagnosed by right heart catheterization when available, or based on high echocardiographic probability or clinician diagnosis when right heart catheterization is not available. Participants should have baseline clinical assessment at or near the time of diagnosis or first presentation and should be able to provide an approximate date or month/year of the first PH-related symptom. Patients with unreliable information regarding symptom onset without alternative documentation, incomplete baseline data preventing assessment of disease severity, acute pulmonary embolism as the sole acute cause of transient pulmonary pressure elevation, or inability to complete the required assessment will be excluded.

Data will be collected using a structured case report form, standardized questionnaire, and review of available clinical records and investigations. Information will include demographic characteristics, residence, occupation, education, smoking status, comorbidities, presenting symptoms, date of first PH-related symptom, date of first medical consultation, initially consulted specialty, number of physicians visited, previous diagnoses, date of first echocardiography, date of suspected PH diagnosis, date of confirmed diagnosis, and patient-reported reasons for diagnostic delay.

Clinical assessment will include symptoms and signs of right-sided heart failure, WHO functional class, vital signs, oxygen saturation, relevant comorbidities, and medications. Functional capacity will be assessed using the six-minute walk distance when available. Available laboratory investigations, particularly hemoglobin and serum creatinine, will be recorded.

Available baseline echocardiographic data will be reviewed, including right atrial size, right ventricular basal diameter, RV systolic function, TAPSE, TR velocity, estimated pulmonary artery systolic pressure, IVC diameter and collapsibility, pericardial effusion, LV ejection fraction, LV diastolic function, left atrial size, valvular disease, and congenital shunts when present.

Right heart catheterization data will be recorded when available as part of routine clinical care, including right atrial pressure, right ventricular pressure, pulmonary artery pressures, pulmonary artery wedge pressure, pulmonary vascular resistance, cardiac output, cardiac index, pulmonary artery/mixed venous oxygen saturation, systemic blood pressure, and vasoreactivity testing results. Right heart catheterization will not be performed solely for research purposes.

The primary outcome will be advanced disease at initial presentation, defined as WHO functional class III-IV. Secondary outcomes will include six-minute walk distance below 300 meters, TAPSE below 17 mm, moderate or severe RV systolic dysfunction, moderate or severe right atrial or right ventricular dilatation, moderate or severe tricuspid regurgitation, pericardial effusion, clinical signs of right-heart failure, hospitalization before diagnosis, and high-risk right heart catheterization features such as elevated right atrial pressure, low cardiac index, and high pulmonary vascular resistance.

Exploratory outcomes will include the number of physicians visited before diagnosis, the first specialty consulted, initial misdiagnosis, and patient-reported causes of diagnostic delay.

Data will be analyzed using appropriate statistical methods. Categorical variables will be compared using the Chi-square or Fisher's exact test, while continuous variables will be analyzed using the independent-samples t-test or Mann-Whitney U test according to data distribution. Correlation analysis will assess the relationship between diagnostic delay in months and continuous severity markers. Multivariable logistic regression will be used to identify independent predictors of advanced disease presentation, with WHO functional class III-IV as the dependent variable. Odds ratios with 95% confidence intervals will be reported, and a two-sided p-value <0.05 will be considered statistically significant.

Medical records will be used whenever possible to verify important dates and investigation results in order to reduce recall bias. No additional invasive procedure will be performed solely for research purposes, and all investigations will be recorded only when performed as part of routine clinical care.

Keywords
Pulmonary hypertension, delayed diagnosis, disease severity
Medical subject headings
Hypertension, Pulmonary

What participants receive

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

Study groups in NCT07810881
Study groupRoleWhat they receive
Pulmonary Hypertension PatientsAdult patients with pulmonary hypertension who fulfill the predefined inclusion criteria and are consecutively recruited for assessment of diagnostic delay and disease severity at initial presentation. Data will be collected through structured questionnaires, clinical assessment, review of medical records, and available investigations.

What is being measured

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

  1. Advanced disease at initial presentation

    The primary outcome is the difference in the proportion of patients with WHO functional class III-IV between the early- and delayed-diagnosis groups at the initial presentation.

    Measured: at the time of diagnosis.

  2. Advanced disease at initial presentation

    The primary outcome is the difference in the proportion of patients with WHO functional class III-IV between the early- and delayed-diagnosis groups at the initial presentation

    Measured: At the initial presentation

Timeline

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

  1. First posted9 Sep 2026
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion1 Nov 2027 (estimated)
  4. Study completion1 Dec 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
Case only
Time perspective
Cross-sectional
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07810881
Sponsor's protocol ID
Diagnostic delay in PHTN
Status last verified
Sep 2026
First submitted
4 Sep 2026
Last updated
9 Sep 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: There is no plan to share individual participant-level data (IPD). Data will be kept confidential and will be accessible only to the research team.

Publications

  • 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 Heart J. 2022 Oct 11;43(38):3618-3731. doi: 10.1093/eurheartj/ehac237. No abstract available.

    PubMed 36017548

Questions about this trial

What is this clinical trial studying?

An observational study of Delayed Diagnosis Pulmonary Hypertension, run by Assiut University.

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: opening soon, as of the sponsor's last update on 9 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

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?

Contact Abanoub Felemon (+201283656965, Bebomessi30@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Advanced disease at initial presentation (time frame: at the time of diagnosis.). The study lists 2 primary outcomes in all. 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 NCT07810881, which also lists 1 linked publication.

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 9 Sep 2026.

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