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An observational study assessing the transition from Ambrisentan to Bosentan in patients with pulmonary arterial hypertension

An observational study assessing the transition from Ambrisentan to Bosentan in patients with pulmonary arterial hypertension

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900025197
Enrollment
Unknown
Registered
2019-08-16
Start date
2018-10-01
Completion date
Unknown
Last updated
2019-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pulmonary artery hypertension

Interventions

Case series:drug transition

Sponsors

Second Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years old; 2. diagnosed of Pulmonary artery hypertension by right heart catheter:mean pulmonary pressure >=25mmHg,pulmonary capillary wedge pressure or end diastolic pressure of left ventrical3 wood; 3. take Bosentan for more than 6 months and had no drug transition in the past 6 months; 4. have no dysfuction of liver and renal function, or below the 3 times of the normal upper line; 5. Consider of transition from Bosentan to Ambrisentan because of financial burden.

Exclusion criteria

Exclusion criteria: 1. Risk stratification of the patients were high; 2. patients who have impairment of renal,liver and thyroid function(more than three times of normal upper limit) or have severe infection; 3. Change of treatment plan within 6 month, or have bosentan for less than 6 months; 4. Have no intention to participate or a low compliance.

Design outcomes

Primary

MeasureTime frame
6 minite walking distance;echocardiography;NT-proBNP;SATMED-Q Scale;

Countries

China

Contacts

Public ContactJiang Li

Second Xiangya Hospital of Central South University

lijiangcs@163.com+86 13975128898

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026