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Sponsors and Collaborators: |
Lund University Hospital Bayer |
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Information provided by: | Lund University Hospital |
ClinicalTrials.gov Identifier: | NCT00216931 |
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 |
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Persistent Pulmonary Hypertension Respiratory Distress Syndrome |
Drug: iloprost |
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 |
Ages Eligible for Study: | up to 48 Hours |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Vineta Fellman, Professor | +46 46 172698 | Vineta.Fellman@med.lu.se |
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 |
Principal Investigator: | Vineta Fellman, Professor | Lund University Hospital, Department of Pediatrics |
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 |
Iloprost Respiratory Tract Diseases Hypertension, Pulmonary Lung Diseases Respiration Disorders |
Respiratory Distress Syndrome, Adult Vascular Diseases Acute respiratory distress syndrome Hypertension |
Vasodilator Agents Pathologic Processes Disease Therapeutic Uses Syndrome |
Hematologic Agents Platelet Aggregation Inhibitors Cardiovascular Diseases Cardiovascular Agents Pharmacologic Actions |