- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07577414
Safety and Efficacy of Fetoscopic Endoluminal Tracheal Occlusion (FETO) in Congenital Diaphragmatic Hernia (CDH)
26. juni 2026 oppdatert av: 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.
Studieoversikt
Status
Rekruttering
Forhold
Studietype
Intervensjonell
Registrering (Antatt)
40
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Erin Perrone, MD
- Telefonnummer: 734-936-8464
- E-post: eperrone@med.umich.edu
Studer Kontakt Backup
- Navn: Irene Carter
- Telefonnummer: 734-615-3883
- E-post: irenestc@med.umich.edu
Studiesteder
-
-
Michigan
-
Ann Arbor, Michigan, Forente stater, 48109
- Rekruttering
- University of Michigan
-
Ta kontakt med:
- Irene Carter
- Telefonnummer: 734-615-3883
- E-post: irenestc@med.umich.edu
-
Hovedetterforsker:
- Erin Perrone, MD
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Beskrivelse
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
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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.
|
Dette vil finne sted mellom svangerskapet 27w0d - 29w6d.
Ballongen vil bli fjernet ved ca. 34 ukers svangerskap.
|
|
Ingen inngripen: 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.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Compare neonatal survival to discharge in LCDH
Tidsramme: 6-12 months (birth to discharge)
|
6-12 months (birth to discharge)
|
|
|
Compare neonatal survival to discharge in RCDH
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Fetal lung growth difference on MRI via o/e Total Fetal Lung Volume (TFLV) (FETO Intervention Arm)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: After birth at 2 months
|
After birth at 2 months
|
|
|
Infant sepsis
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Hovedetterforsker: Erin Perrone, MD, University of Michigan
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
17. juni 2026
Primær fullføring (Antatt)
1. april 2036
Studiet fullført (Antatt)
1. april 2038
Datoer for studieregistrering
Først innsendt
3. mai 2026
Først innsendt som oppfylte QC-kriteriene
3. mai 2026
Først lagt ut (Faktiske)
11. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
29. juni 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
26. juni 2026
Sist bekreftet
1. juni 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- HUM00265099
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Ja
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .