Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
15 participants
INTERVENTIONAL
2022-04-01
2024-03-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Phenotyping of the Out-of-proportion Pulmonary Hypertension
NCT06051396
Prognosis of Coronavirus Disease 2019 (COVID-19) Patients Receiving Receiving Antihypertensives
NCT04357535
Covid-19 Patients With Hypertension and/or Kidney Diseases
NCT05465772
N-terminal Pro B-type Natriuretic Peptide and Vitamin D Levels as Prognostic Markers in COVID-19 Pneumonia
NCT04487951
Hypertension in Patients Hospitalized With COVID-19
NCT04318301
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
According to the 6th World Symposium on Pulmonary Hypertension, pulmonary hypertension (PH) is defined by mean pulmonary arterial pressure (mPAP) \>20 mmHg. "Pre-capillary PH" is considered if additionally pulmonary arterial wedge pressure (PAWP) is ≤15 mmHg and pulmonary vascular resistance (PVR) is ≥3 Wood units (WU). "Post-capillary PH" is defined as mPAP \>20 mmHg with PAWP \>15 mmHg. In the case of PVR \<3 WU, we talk about "isolated post-capillary PH", while in the case of PVR ≥3 WU the criteria for "combined pre- and post-capillary PH" are fulfilled. Post COVID-19 pulmonary hypertension can develop as a result of lung parenchymal damage and altered pulmonary circulation induced by COVID-19 infection. It has been proposed that this type of PH should be considered a combination between PH of group 3 (due to interstitial fibrosis and alveolar inflammation) and 4 (induced by thrombotic/thromboembolic processes, endothelial injury, or, at least, hypoxic vasoconstriction). Right heart catheterization (RHC) is the gold standard for assessing pulmonary hemodynamics and is mandatory for confirming the diagnosis of pulmonary hypertension (PH), assessing the severity of hemodynamic impairment, and performing vasoreactivity testing in selected patients.
Hypothesis and assumptions:
We hypothesize that pulmonary hypertension explain some of residual symptoms in COVID-19 survivors.
Aim of work:
The aim of this study is to assess pulmonary hemodynamics in COVID-19 survivors.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
assess pulmonary hemodynamics in COVID-19 survivors
COVID-19 survivors from a moderate/severe COVID-19 pulmonary infection according to WHO COVID-19 clinical severity classification, ≥ 18 years, with residual symptoms and signs suggestive of pulmonary hypertension and not explained by other condition
right heart catheterization (RHC).
Assessment of pulmonary artery pressure in COVID-19 survivors using right heart catheterization (RHC).
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
right heart catheterization (RHC).
Assessment of pulmonary artery pressure in COVID-19 survivors using right heart catheterization (RHC).
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Hemodynamic instability.
* Absolute contraindications to RHC placement include:
* Infection at the insertion site.
* The presence of a right ventricular assist device.
* Insertion during cardiopulmonary bypass.
* Lack of consent.
* Relative contraindications to RHC placement include:
* Coagulopathy (INR \>1.5), thrombocytopenia (platelet count \<50,000/microL).
* Electrolyte disturbances.
* Severe acid-base disturbances.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Mansoura University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mohamed Abd Elmoniem Mohamed
Assistant lecturer chest medicine-Mansoura univerisity-Mansoura-Egypt
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Mohamed Abd Elmoniem
Role: STUDY_DIRECTOR
assistant lecturer chest medicine Mansoura university
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
faculty of medicine Mansoura university
Al Mansurah, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
MD.22.04.638
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.