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OpenTrials
Completed

NCT Number: NCT01281371

Observation Study of the Medication Switch at Patients Treated With Sitaxentan to a Regime Without Sitaxentan

Due to the withdrawal of Thelin (Sitaxentan) in December 2010 all patients with pulmonary hypertension treated with Sitaxentan need to be switched to an alternative therapy. This study will observe in which way the change of medication - in the clinical routine, without exception in charge of the treating physician - affects clinical and laboratory parameters and patient's quality of life.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Clinical Pharmacology and Pharmacoepidemiology, Medical department of the University of Heidelberg

Heidelberg, Baden-Wurttemberg, 69120, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pulmonary hypertension
  • Treatment with Sitaxentan

Exclusion criteria

  • Inability or unwillingness to give written informed consent

Sponsors and collaborators

Lead sponsor

Heidelberg University

Other

Registry information

Official study title

Clinical Devolution of a Medication Change at Patients With Mono- or Combination Therapy With Sitaxentan to a Regime Without Sitaxentan.

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Jan 21, 2011
Registry last updated
Jun 27, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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