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| Name | Class |
|---|---|
| Allina Health System | OTHER |
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This is a single site pilot trial to study the feasibility of Fetoscopic Endoluminal Tracheal Occlusion (FETO) therapy in the most severe group of fetuses with congenital diaphragmatic hernia (CDH) at Midwest Fetal Care Center, a collaboration between Allina Health and Children's Minnesota. This procedure aims to increase fetal lung volume before birth and improve survival after birth. This study will enroll 10 pregnant people and their baby who meet study criteria.
This is a single site pilot trial to assess the feasibility and safety of treating the most severe group of fetuses with left CDH with Fetal Endoluminal Tracheal Occlusion (FETO) using the Goldballoon Detachable Balloon (GOLDBAL2) along with the Delivery Microcatheter (BALTACCI-BDPE100) at Midwest Fetal Care Center (MWFCC), a collaboration between Allina Health and Children's MN.
Congenital Diaphragmatic Hernia (CDH) is a condition in which a hole in the baby's diaphragm allows the abdominal organs to move into the chest and limit lung growth. The goal of the FETO device is to block the airway with a balloon-type device, allowing fluid to build up in the lungs and help the unborn baby's lungs grow. Bigger lungs may improve the baby's quality of life. The rationale for fetal therapy in severe CDH is to improve fetal lung growth and therefore neonatal survival.
The study will enroll pregnant women that meet study criteria, and their baby. The mother-fetus participant will undergo one procedure for placement of FETO before gestational age 29 weeks 6 days; and a second procedure for removal of the FETO device. The timing for removal of FETO is no later than 35 weeks and 6 days. After delivery, routine care of the baby with CDH will occur within the Children's MN NICU.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| FETO therapy | Experimental | FETO therapy |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| FETO therapy | Device | placement of FETO prior to 29 weeks 6 days GA; and removal of the FETO device no later than 35 weeks and 6 days |
|
| Measure | Description | Time Frame |
|---|---|---|
| Successful placement of Balt Goldbal2 balloon | Successful completion of balloon insertion in fetuses with severe CDH defined as direct visualization of balloon above the carina at the time of FETO procedure. | Prior to 29 weeks 6 days Gestational Age (GA) |
| Successful removal of Balt Goldbal2 balloon | Removal of the balloon | Prior to 35 weeks 6 days GA |
| Measure | Description | Time Frame |
|---|---|---|
| Change in fetal lung growth | Prenatal ultrasound will measure the observed-to-expected lung to head ratio (o/e LHR) at weekly visits while the balloon is in place and after balloon removal. Fetal lung growth will be calculated as the difference between the o/e LHR pre-balloon placement and the o/e LHR after balloon removal. | Immediately after intervention (device removal) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| James E Fisher, MD | Contact | 612.863.9924 | jfisher@pediatricsurgical.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Midwest Fetal Care Center | Recruiting | Minneapolis | Minnesota | 55404 | United States |
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| ID | Term |
|---|---|
| D006548 | Hernia, Diaphragmatic |
| ID | Term |
|---|---|
| D000082122 | Internal Hernia |
| D006547 | Hernia |
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| Gestational age at delivery | Gestational age at delivery will be recorded. | Measured at time of delivery |
| Infant survival | Infant survival will be recorded from delivery to NICU discharge, and at 6, 12, and 24 months of age | Birth - 24 months |
| Number of infants requiring extra corporeal membrane oxygenation (ECMO) support | Use of ECMO will be collected from medical chart review. | Birth to 6 months |
| Number of infants requiring tracheostomy while in the NICU | Tracheostomy information will be collected from medical chart review. | up to 2 years of age |
| Number of infants requiring home oxygen support upon discharge from the NICU | Oxygen support will be collected from medical chart review. | up to 2 years of age |
| Time to pulmonary hypertension resolution | pulmonary hypertension will be collected from medical chart review. | up to 2 years of age |