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Treatment of Elevated Arterial Pulmonary Pressure With Inhaled Iloprost
This study is currently recruiting participants.
Verified by Lund University Hospital, September 2007
Sponsors and Collaborators: Lund University Hospital
Bayer
Information provided by: Lund University Hospital
ClinicalTrials.gov Identifier: NCT00216931
  Purpose

The purpose of this study is to determine if iloprost is effective in the treatment of elevated arterial pulmonary pressure in children with ventilator treated respiratory distress syndrome.


Condition Intervention
Persistent Pulmonary Hypertension
Respiratory Distress Syndrome
Drug: iloprost

Genetics Home Reference related topics: pulmonary arterial hypertension
MedlinePlus related topics: High Blood Pressure Pulmonary Hypertension
Drug Information available for: Iloprost
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Official Title: Treatment of Elevated Arterial Pulmonary Pressure With Inhaled Iloprost

Further study details as provided by Lund University Hospital:

Primary Outcome Measures:
  • Oxygenation index
  • Cardiac output

Estimated Enrollment: 40
Study Start Date: May 2006
Estimated Study Completion Date: October 2008
  Eligibility

Ages Eligible for Study:   up to 48 Hours
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Elevated arterial pulmonary pressure
  • GA > 24 GW
  • 24-48 hours of age
  • Ventilator treatment

Exclusion Criteria:

  • Congenital anomalies
  • Severe hypotension
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00216931

Contacts
Contact: Vineta Fellman, Professor +46 46 172698 Vineta.Fellman@med.lu.se

Locations
Sweden
University Hospital in Lund , Department of Pediatrics Recruiting
Lund, Sweden, 221 85
Contact: Anders Nordh, MD     +46 46178446     anders.nordh@skane.se    
Principal Investigator: Anders Nordh, MD            
Sponsors and Collaborators
Lund University Hospital
Bayer
Investigators
Principal Investigator: Vineta Fellman, Professor Lund University Hospital, Department of Pediatrics
  More Information

Study ID Numbers: 2004-001551-11
Study First Received: September 15, 2005
Last Updated: December 10, 2007
ClinicalTrials.gov Identifier: NCT00216931  
Health Authority: Sweden: Medical Products Agency

Study placed in the following topic categories:
Iloprost
Respiratory Tract Diseases
Hypertension, Pulmonary
Lung Diseases
Respiration Disorders
Respiratory Distress Syndrome, Adult
Vascular Diseases
Acute respiratory distress syndrome
Hypertension

Additional relevant MeSH terms:
Vasodilator Agents
Pathologic Processes
Disease
Therapeutic Uses
Syndrome
Hematologic Agents
Platelet Aggregation Inhibitors
Cardiovascular Diseases
Cardiovascular Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 14, 2009