Connective Tissue Disease Patients With Pulmonary Hypertension

Sponsor
The First Affiliated Hospital with Nanjing Medical University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05980728
Collaborator
(none)
500
84

Study Details

Study Description

Brief Summary

Adult patients with suspected or confirmed Connective Tissue Disease Patients (CTD)With Pulmonary Hypertension(PH)will be recruited. Patients will be approached, consented, have baseline demographics, diagnostics and disease activity measures recorded, and blood taken. The collection of data and biological material will mirror usual clinical practice as far as possible. Subjects will ideally attend further visits at 3, 6 and 12 months to have bloods taken, outcome measures recorded and questionnaires completed.

Condition or Disease Intervention/Treatment Phase
  • Other: No Intervention

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
500 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Prognostic Value of Biomarker in Connective Tissue Disease Patients With Pulmonary Hypertension
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Sep 1, 2027
Anticipated Study Completion Date :
Sep 1, 2030

Arms and Interventions

Arm Intervention/Treatment
Connective Tissue Disease Patients With Pulmonary Hypertension

Connective Tissue Disease Patients With Pulmonary Hypertension

Other: No Intervention
No Intervention

Connective Tissue Disease Patients Without Pulmonary Hypertension

Connective Tissue Disease Patients Without Pulmonary Hypertension

Other: No Intervention
No Intervention

healthy

healthy people

Other: No Intervention
No Intervention

Outcome Measures

Primary Outcome Measures

  1. Death [30 years]

    number of participants with All cause death

Secondary Outcome Measures

  1. Clinical worsening [30 years]

    number of participants with Hospitalization for worsening pulmonary arterial hypertension(PAH),lung or heart/lung transplant) or unsatisfactory long-term clinical response (the 6-minute walk distance decreased > 15% from baseline and World Health Organization(WHO) functional class III/IV symptoms assessed at two clinic visits separated by > 6 months after sufficient PAH targeted drug treatment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Definite diagnosis of CTD included Systemic lupus erythematosus(SLE) diagnosed according to the 2019 The European Alliance of Associations for Rheumatology(EULAR) criteria, primary Sjogren's syndrome (pSS) defined according to the 2016 American College of Rheumatology(ACR) criteria, Systemic Sclerosis(SSc) defined according to the 2013 ACR criteria, mixed connective tissue disease (MCTD) defined by Sharp criteria, and Rheumatoid Arthritis(RA) defined according 2010 ACR criteria of two or more CTD at the same time were defined as having overlap syndrome (OS). Patients who had clinical and serological manifestations suggestive of systemic autoimmune diseases but did not fulfil the classification criteria for CTD were defined as having undifferentiated CTD (UCTD).

  • PAH was diagnosed by right heart catheterization was defined as mean Pulmonary Artery Pressure (mPAP)>20 Millimeters of mercury(mmHg), Pulmonary Artery Wedge Pressure(PAWP)≤15mmHg, Pulmonary Vascular Resistance(PVR)>2 Wood

Exclusion Criteria:
  • significant interstitial lung disease or chronic obstructive pulmonary disease;

  • left heart disease or congenital heart disease associated with pulmonary hypertension;

  • chronic thromboembolic pulmonary hypertension;

  • portal hypertension;

  • drug or toxin exposure;

  • HIV infection;

  • any other diseases known to be associated with PAH;

  • age<18 years.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • The First Affiliated Hospital with Nanjing Medical University

Investigators

  • Principal Investigator: Qiang Wang, MD, The First Affiliated Hospital with Nanjing Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
The First Affiliated Hospital with Nanjing Medical University
ClinicalTrials.gov Identifier:
NCT05980728
Other Study ID Numbers:
  • JSPH cohort
First Posted:
Aug 8, 2023
Last Update Posted:
Aug 8, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by The First Affiliated Hospital with Nanjing Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 8, 2023