Immune clues in rare lung disease explored
NCT ID NCT01208792
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed study looked at how the immune system might affect the outlook for people with pulmonary arterial hypertension (PAH). Researchers took blood and skin samples from 629 participants with different types of PAH to search for specific antibodies. The goal was to better understand the role of autoimmunity in the disease.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this research could help identify immune markers that predict disease progression in pulmonary arterial hypertension.
- What could go wrong
- This is an observational study, not a treatment trial. Findings may not lead to direct therapies or apply to all patient groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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629 people
The number who actually took part.
- Started
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Jun 2010
- Finished
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May 2017
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: age over 18 * for PAH patients: pre-capillary PAH evidenced by right-heart catheterization * no associated systemic disease for idiopathic PAH patients * for HIV patients, HIV1 infection confirmed by ELISA and western blot * for patients with porto pulmonary hypertension: evidence by endoscopy of esophageal varices, confirmation of hepatic venous pressure gradient over 5 mmHg by catheterization of the hepatic veins * for patients with congenital heart defect: evidence by imaging of atrial or ventricular septal defect, or patent ductus arterious and confirmed by heart catheterization * patients with SSc will fulfill the American College of Rheumatology (ACR) and the LEROY and MEDSGER criteria * patients with MCTD will fulfill the criteria for MCTD * patients with SLE will fulfill the updated and revised ACR criteria * patients with Sjögren's syndrome will fulfill the American-European consensus group criteria * patients with chronic thromboembolic pulmonary hypertension: Lung scintiscan showing segmental mismatched perfusion defects and confirmation by angiography of the occlusion and the chance of success of endarterectomy according to the location of disease * Signed written informed consent * Patients with health insurance Exclusion Criteria: * age under 18 * pregnant women * absence of written informed consent * associated malignant tumor
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Internal Medicine Department, Claude Huriez Hospital
Lille, 59000, France
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Internal Medicine Department, Cochin Hospital
Paris, 75014, France
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Pneumology Department, Antoine Béclère Hospital
Clamart, 92000, France
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