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Safety and Efficacy of Fetoscopic Endoluminal Tracheal Occlusion (FETO) in Congenital Diaphragmatic Hernia (CDH)

26 juni 2026 bijgewerkt door: Dr Erin Perrone

Infant Survival and Long-term Outcome Following Fetoscopic Endoluminal Tracheal Occlusion in Severe Left and Right Congenital Diaphragmatic Hernia, A Phase III Trial

The purpose of the study is to determine if babies with left or right-sided CDH that undergo the FETO procedure survive more often and have fewer long-term complications than babies that have similar left or right-sided CDH that elect not to have the FETO procedure performed during pregnancy.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Geschat)

40

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Contact Back-up

Studie Locaties

    • Michigan
      • Ann Arbor, Michigan, Verenigde Staten, 48109
        • Werving
        • University of Michigan
        • Contact:
        • Hoofdonderzoeker:
          • Erin Perrone, MD

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

FETO Intervention Arm: Inclusion Criteria:

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability (meets psychosocial criteria below) for the duration of the study
  • Pregnant women, age 18 years and older
  • Singleton pregnancy
  • Normal fetal karyotype, Chromosomal Microarray (CMA) with non-pathologic variants, Whole Exome Sequencing (WES) or Whole Genome Sequencing (WGS). Results by fluorescence in situ hybridization (FISH) will be acceptable if the patient is >26 weeks.
  • Gestational age at enrollment prior to 29w6d
  • Fetal CDH with intrathoracic liver herniation with either:

    • Isolated left CDH with Observed/Expected (o/e) Lung to Head Ratio (LHR) <30% at enrollment (18w0d-29w5d)
    • Isolated right CDH with o/e LHR <45% at enrollment (18w0d-29w5d)
  • Cervical length by transvaginal ultrasound >20 mm within 24hours of FETO procedure
  • Meets psychosocial criteria

    • Willing to reside within 30 minutes of Von Voigtlander Women's Hospital and ability to maintain follow up appointments
    • Patient has a support person (e.g. spouse, partner, friend, parent) that is available to stay with participant for the duration of the pregnancy near Von Voigtlander Women's Hospital
    • Willing to comply with restrictions of daily living including inability to exercise, have intercourse, or return to work (work from home approved by Principal Investigator is okay)

Expectant Management Arm: Inclusion Criteria:

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability (meets psychosocial criteria below) for the duration of the study
  • Pregnant women, age 18 years and older
  • Singleton pregnancy
  • Normal fetal karyotype, CMA with non-pathologic variants, WES or WGS. Results by fluorescence in situ hybridization (FISH) will be acceptable if the patient is >26 weeks. (non-intervention arm can have karyotype or microarray prenatally or postnatally)
  • Gestational age at enrollment prior to 29w6d
  • Fetal CDH with intrathoracic liver herniation with either:
  • Isolated left CDH with o/e LHR <30% at enrollment (18w0d-29w5d)
  • Isolated right CDH with o/e LHR <45% at enrollment (18w0d-29w5d)
  • Meets psychosocial criteria

    • Ability to maintain follow up appointments

FETO Intervention Arm: Exclusion Criteria:

  • Patient <18 years of age
  • Multi-fetal pregnancy
  • History of natural rubber latex allergy
  • Preterm labor, short cervix (<20mm within 24 hours of FETO balloon insertion procedure), or uterine anomaly strongly predisposing to preterm labor, placenta previa
  • History of incompetent cervix with or without cerclage
  • Psychosocial ineligibility

    • Inability to reside within 30 minutes of Von Voigtlander Women's Hospital or inability to maintain follow up appointments
    • Social work will meet with each patient to evaluate the social situation and support system. Identifiable issues of social instability or compliance with the protocol will exclude participant as a potential candidate (per protocol).
  • Bilateral CDH, isolated Left Congenital Diaphragmatic Hernia (LCDH) with o/e LHR > 30% (measured at 180 to 295 weeks), isolated Right Congenital Diaphragmatic Hernia (RCDH) with o/e LHR >45% (measured at 180 to 295 weeks) as determined by ultrasound
  • No liver herniation into the thoracic cavity.
  • Additional fetal anomaly or genetic/chromosomal abnormalities recognized to alter survival prognosis (i.e., congenital heart disease) or presence of an underlying genetic syndrome (i.e. Fryns) by ultrasound, MRI or echocardiogram at the fetal treatment center.
  • Maternal contraindications to elective fetoscopic surgery or severe maternal medical condition in pregnancy
  • Placental abnormalities (previa, abruption, accreta) known at time of enrollment and/or surgery
  • Maternal-fetal Rh isoimmunization, Kell sensitization, or neonatal alloimmune thrombocytopenia affecting the current pregnancy
  • Maternal Human Immunodeficiency Virus (HIV), Hepatitis B with positive surface antigen, Hepatitis C with presence of virus in maternal blood due to risk of fetal transmission during the procedure. If the patient's HIV or Hepatitis status is unknown, the patient must be tested and found to have negative results before enrollment
  • No safe or technically feasible fetoscopic approach to balloon placement
  • Uterine anomalies such as large fibroids or Mullerian duct abnormality
  • Participation in another intervention study that influences maternal and fetal morbidity and mortality or participation in this trial in a previous pregnancy

Expectant Management Arm: Exclusion Criteria:

  • Patient <18 years of age
  • Multi-fetal pregnancy
  • Preterm labor, short cervix (<20mm), or uterine anomaly strongly predisposing to preterm labor, placenta previa
  • History of incompetent cervix with or without cerclage
  • Psychosocial ineligibility

    • Inability to maintain follow up appointments
    • Social work will meet with each patient to evaluate the social situation and support system. Identifiable issues of social instability or compliance with the protocol will exclude participant as a potential candidate.
  • Bilateral CDH, isolated LCDH with o/e LHR > 30% (measured at 180 to 295 weeks), isolated RCDH with o/e LHR >45% (measured at 180 to 295 weeks), or any isolated CDH without intrathoracic liver herniation as determined by ultrasound
  • Additional fetal anomaly or genetic/chromosomal abnormalities recognized to alter survival prognosis (i.e. congenital heart disease) or presence of an underlying genetic syndrome (i.e. Fryns) by ultrasound, Magnetic Resonance Imaging (MRI) or echocardiogram at the fetal treatment center Placental abnormalities (per protocol)
  • Participation in another intervention study that influences maternal and fetal morbidity and mortality or participation in this trial in a previous pregnancy

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Niet-gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: FETO surgery Intervention Arm
Eligible participants that choose the FETO Intervention Arm, will undergo two surgeries, one to place the balloon and a second to remove the balloon before delivery.
Dit vindt plaats tussen de zwangerschap van 27w0d - 29w6d. De ballon wordt bij ongeveer 34 weken zwangerschap verwijderd.
Geen tussenkomst: Expectant Management Arm
Participants choose to undergo the expectant management, or routine care, of carrying a baby with Congenital Diaphragmatic Hernia (CDH). Participants will undergo a comprehensive fetal evaluation at Michigan Medicine's Fetal Diagnosis and Treatment Center (FDTC) to confirm the diagnosis and severity of the CDH. Eligibility will be based on the results of the clinical assessment.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Compare neonatal survival to discharge in LCDH
Tijdsspanne: 6-12 months (birth to discharge)
6-12 months (birth to discharge)
Compare neonatal survival to discharge in RCDH
Tijdsspanne: 6-12 months (birth to discharge)
6-12 months (birth to discharge)
Number of successful placements the of FETO balloon Gestational age of 27 weeks 0 days gestation to 29 weeks 6 days gestation
Tijdsspanne: 27weeks 0 days gestation to 29 weeks 6 days gestation
27weeks 0 days gestation to 29 weeks 6 days gestation
Number of successful retrievals/puncture of the FETO balloon Gestational age of 33 weeks 0 days to 35 weeks 0 days
Tijdsspanne: Removal prior to delivery at approximately 34 weeks of gestation
Removal prior to delivery at approximately 34 weeks of gestation
Number of FETO procedure complications
Tijdsspanne: Balloon placement to delivery (27 weeks up to delivery approximately 40 weeks)
FETO procedure complications include: Failure of the FETO insertion procedure; FETO device dislodgement potentially requiring a second FETO insertion; Fetal intraoperative injury; Procedural hemorrhage: Bleeding from insertion site or Abruptions; Post-procedural hemorrhage; Preterm premature rupture of membranes; Preterm delivery; Chorioamnion separation; Chorioamnionitis; Polyhydramnios; Oligohydramnios; Emergent removal due to obstetrical complication; Failed percutaneous or fetoscopic removal requiring cesarean section or Ex-Utero Intrapartum Therapy(EXIT) procedure for removal; Neonatal death due to asphyxia if delivery before FETO removal; Non-reassuring fetal heart rate monitoring.
Balloon placement to delivery (27 weeks up to delivery approximately 40 weeks)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Fetal lung growth difference on MRI via o/e Total Fetal Lung Volume (TFLV) (FETO Intervention Arm)
Tijdsspanne: Baseline (prior to balloon placement) and approximately 2 weeks after balloon retrieval
Fetal MRI done prior to balloon placement and again done at approximately 2 weeks of balloon retrieval. Fetal lung growth (difference between 1st and 2nd MRIs will be calculated for FETO intervention arm only).
Baseline (prior to balloon placement) and approximately 2 weeks after balloon retrieval
Fetal lung growth difference based on prenatal ultrasound via o/e LHR (Both Arms)
Tijdsspanne: Baseline (prior to balloon placement) and immediately prior to balloon removal and SOC arm 29 + 1 week and 34 +1 week
Prenatal ultrasound (US) will measure the o/e LHR at weekly visits while the balloon is in place (FETO intervention arm) or at routine visits per standard of care (SOC) (expectant arm). Fetal lung growth will be calculated as the difference between the o/e LHR pre- balloon placement (or 29 + 1 week in control) and the o/e LHR immediately prior to balloon removal/puncture (or 34 + 1 week in control).
Baseline (prior to balloon placement) and immediately prior to balloon removal and SOC arm 29 + 1 week and 34 +1 week
Long-term outcome measure infant survival rate
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Presence of pulmonary hypertension
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Determination of the ratio of the tricuspid regurgitation jet (estimation of the right ventricular systolic pressure) to systemic blood pressure where the is an objective measurement used to estimate the pulmonary artery pressure. Will be recorded as absent/none, systemic or suprasystemic.
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Presence of need for supplemental oxygen
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Periventricular leukomalacia at <2 months postnatally
Tijdsspanne: After birth at 2 months
After birth at 2 months
Infant sepsis
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Intraventricular hemorrhage (grade 0-III)
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Retinopathy of prematurity (grade 3 or higher)
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Gastroesophageal reflux
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Number and cause of infant hospital readmissions
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Long-term outcome measure childhood growth failure
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Childhood growth failure: weight gain velocity or decline >2 in weight, for length Z score.
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Recurrence of CDH repair
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
Bowel obstruction
Tijdsspanne: After birth at 6, 12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6, 12, 18, and 24 months (+ 2 months) of corrected age
Neurodevelopmental delay
Tijdsspanne: 24 months (+ 2 months) of corrected age
Bayley Scales of Infant and Toddler Development- III(BSID)>2 Standard deviation (SD) below mean, or other categorization at 24 months
24 months (+ 2 months) of corrected age
Bronchopulmonary dysplasia
Tijdsspanne: After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age
After birth at 6,12, 18, and 24 months (+ 2 months) of corrected age

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Onderzoekers

  • Hoofdonderzoeker: Erin Perrone, MD, University of Michigan

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

17 juni 2026

Primaire voltooiing (Geschat)

1 april 2036

Studie voltooiing (Geschat)

1 april 2038

Studieregistratiedata

Eerst ingediend

3 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

3 mei 2026

Eerst geplaatst (Werkelijk)

11 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

29 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

26 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Ja

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