Congenital Diaphragmatic Hernia Clinical Trial
Official title:
A Pilot Study on the Role of Fetal Endotracheal Occlusion (FETO) in Fetuses With Severe Congenital Diaphragmatic Hernia
The goal of this pilot trial is to learn more about the role of Fetal Endotracheal Occlusion (FETO) as an intervention in fetuses with severe congenital diaphragmatic hernia (CDH). The research team will investigate the feasibility and safety of the FETO procedure, as well as determine whether FETO can improve lung growth before birth, and survival after birth. This study will enroll 10 pregnant participants to undergo the FETO procedure at a gestational age of 27 weeks 0 days to 29 weeks 6 days. The participant will be monitored for a few weeks, and then the FETO removal procedure will be performed ideally at 34 weeks 0 days to 34 weeks 6 days, but may be indicated earlier as determined by the Maternal Fetal care team. The pregnant participant and their baby will continue to be monitored during delivery and up until the child reaches 2 years of age.
Status | Not yet recruiting |
Enrollment | 10 |
Est. completion date | February 28, 2031 |
Est. primary completion date | September 1, 2027 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Pregnant patient 18 and older who is able to consent - Singleton pregnancy - Ability to reside within 30 minutes of Boston Children's Hospital for the duration of the FETO intervention, from the time of balloon placement until balloon removal - Patient has a support person who is able to stay with them for the duration of the pregnancy Fetal: - Reassuring genetic analysis demonstrated by either normal Karyotype, normal fluorescence in situ hybridization (FISH) for chromosomes 13, 18, 21, X and Y, or chromosomal microarray (CMA) with non-pathologic variants - Diagnosis of isolated left CDH with liver up - Gestation at enrollment prior to 29 weeks 5 days - SEVERE pulmonary hypoplasia with ultrasound Observed/Expected Lung-to-Head Ratio (O/E LHR) < 25% Exclusion Criteria: - Maternal contraindication to fetoscopic surgery or severe maternal medical condition in pregnancy - Technical limitations precluding fetoscopic surgery, including uterine anomaly such as large or multiple fibroids, or Mullerian duct anomaly - Latex allergy - Preterm labor, shortened cervix (<20mm at enrollment or within 24 hours of FETO balloon insertion procedure) or uterine anomaly strongly predisposing to preterm labor, placenta previa - Severe maternal obesity pre-pregnancy (BMI > 40) - Psychosocial ineligibility, precluding consent, as determined by clinic social worker during review - Inability to remain at FETO site during time period of tracheal occlusion, delivery, and postnatal care - Right-sided or bilateral, left-sided CDH observed-to-expected lung to head ratio > 25% on ultrasound - Additional fetal anomaly and chromosomal abnormalities by ultrasound, MRI, or echocardiogram that will significantly worsen prognosis - History of incompetent cervix with or without cerclage - Placental abnormalities (previa, abruption, accreta) known at time of enrollment - Maternal-fetal RH (rhesus) isoimmunization, Kell sensitization, or neonatal alloimmune thrombocytopenia affecting the current pregnancy - Maternal HIV, Hepatitis B, Hepatitis C status positive |
Country | Name | City | State |
---|---|---|---|
United States | Boston Children's Hospital | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Alireza Shamshirsaz |
United States,
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* Note: There are 56 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Successful Ballon Placement | Defined as direct visualization of balloon deployment above the carina at the time of FETO procedure | Gestational age of 27 weeks 0 days to 29 weeks 6 days | |
Primary | Successful Balloon Removal | Removal of the balloon prior to delivery, ideally during 34 weeks gestation | Prior to delivery, ideally at 34 weeks | |
Primary | Balloon placement operative time | Length of FETO procedure for successful balloon placement | Gestational age of 27 weeks 0 days to 29 weeks 6 days | |
Primary | Balloon removal operative time | Length of FETO procedure for successful balloon removal | Prior to delivery, ideally at 34 weeks | |
Primary | Type of FETO release | Emergent or non-emergent FETO release | Prior to delivery, ideally at 34 weeks | |
Primary | Maternal Complications | Maternal complications include: preterm labor, premature rupture of membranes, oligohydramnios, polyhydramnios, chorioamnionitis | From balloon placement to delivery | |
Primary | Gestational age at delivery | Gestational age at delivery will be recorded | At delivery | |
Secondary | Fetal lung volume | Fetal lung volume will be monitored on ultrasound | Once per week from balloon placement to removal. This measure will be recorded at earliest gestational age of 27 weeks 0 days, and latest at 34+6/7 weeks' gestation. | |
Secondary | Observed-to-Expected Lung to Head Ratio | 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. | Calculated at balloon removal, ideally at 34 weeks gestation | |
Secondary | Infant survival | Survival at discharge from the hospital, or at 6 months of age if still hospitalized | At hospital discharge or 6 months of age, whichever comes first. Hospital discharge typically occurs at 2-3 months of age | |
Secondary | Oxygen dependency | Infant dependency on oxygen as defined by Bancalari 2001 | At time of discharge, on average at 2-3 months of age | |
Secondary | Number of infants requiring ECMO (extracorporeal membrane oxygenation) | Use of ECMO support will be documented | Birth to 6 months | |
Secondary | NICU (neonatal intensive care unit) stay | Number of days spent in the neonatal intensive care unit | From birth until discharge, at an average of 2-3 months of age | |
Secondary | Ventilator support | Number of days on ventilator support | Up to 2 years of age | |
Secondary | Presence of periventricular leukomalacia | Incidence of periventricular leukomalacia at <2 months postnatally | From birth until 2 months of age | |
Secondary | Presence of neonatal sepsis | Incidence of neonatal sepsis | From birth until 1 month of age | |
Secondary | Presence of intraventricular hemorrhage | Incidence of intraventricular hemorrhage (grade 0-III) | Up to 2 years of age | |
Secondary | Retinopathy of prematurity | Incidence of retinopathy of prematurity (grade III or higher) | From birth to 1 month of age | |
Secondary | Presence of gastro-esophageal reflux | Incidence of gastro-esophageal reflux | From birth until 2 years of age | |
Secondary | CDH repair type | CDH repair type will be documented as patch or muscle flap | Postnatal, at time of CDH repair, typically within 2 weeks of birth | |
Secondary | Pulmonary function | Pulmonary function by spirometry | At discharge around 2-3 months and at one year of age | |
Secondary | Infant Neurodevelopment | Neurodevelopmental testing of the infant using the Bayley-4 | At 6 months, 12 months, and 24 months of age | |
Secondary | Route of delivery | Delivery route will be recorded | At delivery | |
Secondary | Maternal hospitalization | Total days of maternal hospital stay after delivery | From delivery until discharge, around 2-3 months of age |
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