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Clinical Trial Summary

Diaphragmatic hernia detected in fetal life carries a high risk for postnatal demise due to lung underdevelopment. Clinical experience from prospective controlled non-randomized case series with fetoscopic tracheal balloon occlusion has seen improved survival rates in contrast to untreated controls. Therefore, the purpose of this randomized clinical trial is to provide further evidence about the efficacy and safety of the prenatal interventional approach. Primary outcome measure is postnatal survival to discharge from hospital treatment.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00373763
Study type Interventional
Source University Hospital, Bonn
Contact
Status Withdrawn
Phase N/A
Start date January 2007

See also
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Completed NCT04716166 - Incentive Spirometry and Upper Abdominal Laparoscopic Surgery N/A
Not yet recruiting NCT05354505 - Fetal Endoscopic Tracheal Occlusion (FETO) Trial for Congenital Diaphragmatic Hernia (CDH) N/A
Completed NCT01240057 - Tracheal Occlusion To Accelerate Lung Growth (TOTAL) Trial for Severe Pulmonary Hypoplasia Phase 2/Phase 3
Completed NCT02466451 - Study in Children With the Diagnosis of Congenital Diaphragmatic Hernia (CDH) and Oesophageal Atresia (EA) N/A
Recruiting NCT00373438 - Fetoscopic Tracheal Balloon Occlusion in Left Diaphragmatic Hernia Phase 2
Terminated NCT02364843 - A Physiological Study to Determine the Enteral Threonine Requirements in Infants Aged 1 to 6 Months N/A