Clinical Trials Directory

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UnknownNCT05553015

A Real-World Registry Investigating TReprostInil sodiUM in Pulmonary Hypertension (Re-TRIUMPH)

Status
Unknown
Phase
Study type
Observational
Enrollment
450 (estimated)
Sponsor
Chinese Pulmonary Vascular Disease Research Group · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

A Real-World Registry investigate Treprostinil sodium used in patients with Pulmonary Hypertension (Re-TRIUMPH).

Detailed description

This study is a multicenter, prospective, single-arm, observational, real-world study conducted in China. Patients who are at least 18 years of age, have been diagnosed with pulmonary hypertension (PH), agree to participate and meet the eligibility requirement will be enrolled in 20 pulmonary vascular centers across the country for the medically reasonable use of intravenous (or subcutaneous) Treprostinil injections. In the event that eligible patients are enrolled in the study, all aspects will be carried out in an observational manner, and no additional methods or procedures will be necessary. The patient and the physician will jointly determine the clinical management of the patient, including the length of treatment. Patients will be followed up for an observation period of at least 1 year. As part of standard clinical practice, patient data will be collected at the first appointment and every three to six months thereafter. After one year of follow-up, data collection will cease.The main purpose is to evaluate the efficacy and adverse reactions of subcutaneous (intravenous) prostacyclin in the treatment of pulmonary hypertension under current clinical practice. The secondary objectives is to understand the drug treatment plan of treprostinil in clinical practice of patients with pulmonary arterial hypertension in China and to understand the efficacy and adverse reactions of treprostinil in the treatment of patients with different types of pulmonary hypertension.

Conditions

Timeline

Start date
2020-12-24
Primary completion
2025-08-30
Completion
2025-12-31
First posted
2022-09-23
Last updated
2024-01-17

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05553015. Inclusion in this directory is not an endorsement.