NCT06135909

Brief Summary

CHina Registry for the chAracteristics and Management strategieS of patiEnts With Pulmonary Hypertension Using Targeted Therapy (CHASE Study)

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5,000

participants targeted

Target at P75+ for all trials

Timeline
20mo left

Started Jan 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress79%
Jan 2020Dec 2027

Study Start

First participant enrolled

January 1, 2020

Completed
3.9 years until next milestone

First Submitted

Initial submission to the registry

November 12, 2023

Completed
6 days until next milestone

First Posted

Study publicly available on registry

November 18, 2023

Completed
4.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

January 18, 2024

Status Verified

November 1, 2023

Enrollment Period

8 years

First QC Date

November 12, 2023

Last Update Submit

January 16, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Incidence of clinical worsening events 1 year after enrollment

    All-cause death, Pulmonary hypertension progression associated with re-hospitalization, Progress of pulmonary hypertension disease

    1 year after enrollment

Secondary Outcomes (1)

  • Incidence of all-cause death 1,3,5 year(s) after enrollment

    1,3,5 year(s) after enrollment

Study Arms (1)

PH Patients receiving targeted drugs treatment

Patients with pulmonary hypertension receiving targeted drugs treatment

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients with pulmonary hypertension receiving targeted therapy

You may qualify if:

  • Sign informed consent;
  • Between the ages of 18 and 85;
  • Clinical diagnosis of pulmonary hypertension, using or planning to use pulmonary hypertension targeted drugs (including any one or more of the following: prostacyclin analogues, endothelin receptor antagonists, phosphodiesterase inhibitors, soluble guanylate cyclase agonists and prostacyclin receptor agonists).

You may not qualify if:

  • Have a history of mental illness or drug or poison addiction, and can not sign informed consent or can not cooperate with the experimental study;
  • Patients with malignant tumor and other diseases and life expectancy of less than half a year;
  • Short-term (less than 2 weeks) patients taking targeted drugs for pulmonary hypertension

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Center for Respiratory and Pulmonary Vascular Diseases, Fuwai hospital, CAMS & PUMC

Beijing, 100037, China

RECRUITING

MeSH Terms

Conditions

Hypertension, Pulmonary

Condition Hierarchy (Ancestors)

Lung DiseasesRespiratory Tract DiseasesHypertensionVascular DiseasesCardiovascular Diseases

Study Officials

  • Zhihong Liu, M.D., Ph.D

    Chinese Academy of Medical Sciences, Fuwai Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Zhihong Liu, M.D., Ph.D

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
5 Years
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 12, 2023

First Posted

November 18, 2023

Study Start

January 1, 2020

Primary Completion (Estimated)

December 31, 2027

Study Completion (Estimated)

December 31, 2027

Last Updated

January 18, 2024

Record last verified: 2023-11

Locations