Pilot Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) in Severe Left Congenital Diaphragmatic Hernia (CDH)

Sponsor
Hanmin Lee (Other)
Overall Status
Recruiting
CT.gov ID
NCT04583644
Collaborator
(none)
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Study Details

Study Description

Brief Summary

Despite advances in prenatal diagnosis and postnatal therapies, including ECMO (Extracorporeal Membrane Oxygenation), inhaled nitric oxide therapy, and ventilator strategies that minimize ventilator-induced lung injury, morbidity and mortality rates for babies with severe CDH remain high. The rationale for fetal therapy in severe CDH is to promote adequate lung growth for neonatal survival. Prenatal tracheal occlusion obstructs the normal egress of lung fluid during pulmonary development leading to increased lung tissue stretch, increased cell proliferation, and accelerated lung growth. The investigator's goal with this pilot study is to study the feasibility of implementing Fetoscopic Endoluminal Tracheal Occlusion (FETO) therapy in the most severe group of fetuses with left CDH (LHR O/E < 25%).

Condition or Disease Intervention/Treatment Phase
  • Device: Fetoscopic Endoluminal Tracheal Occlusion Surgery
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Pilot Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) in Severe Left Congenital Diaphragmatic Hernia (CDH)
Actual Study Start Date :
Oct 2, 2020
Anticipated Primary Completion Date :
Apr 1, 2027
Anticipated Study Completion Date :
Apr 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: Device - FETO

Fetoscopic Endoluminal Tracheal Occlusion (FETO) surgery and removal of balloon using the BALT GOLDBAL2 balloon and BALTACCIBDPE100 catheter.

Device: Fetoscopic Endoluminal Tracheal Occlusion Surgery
Fetoscopic Endoluminal Tracheal Occlusion (FETO) surgery will be completed at 27 weeks 0 days - 29 weeks 6 days gestation. Fetoscopic removal of the balloon occlusion will be performed at 34 weeks 0 days to 34 weeks 6 days gestation.

Outcome Measures

Primary Outcome Measures

  1. Number of effective placements of balloon to occlude trachea via fetoscopy [Between 27 and 29 weeks gestation]

    Number of effective placements of balloon to occlude trachea via fetoscopy by performing Fetoscopic Endoluminal Tracheal Occlusion (FETO) in fetuses with severe left congenital diaphragmatic hernia (CDH), as defined by lung to head ratio (LHR) Observed/Expected < 25%

Secondary Outcome Measures

  1. Rate of fetal lung growth after FETO as measured by lung volume. [Between 27 and 34 weeks gestation]

    Fetal lung growth as measured by lung volume.

  2. Rate of fetal lung growth after FETO as measured by Lung to head circumference ratio [Between 27 and 34 weeks gestation]

    Fetal lung growth as measured by Lung to head circumference ratio (LHR) measurements.

  3. Determine survival rate of FETO patients [6 months after birth]

    Survival at 6 months after birth.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pregnant women age 18 years and older

  • Singleton pregnancy

  • Normal fetal karyotype with confirmation by culture results. Results by fluorescence in situ hybridization (FISH) will be acceptable if the patient is > 26 weeks

  • Isolated Left CDH with liver up

  • Gestation age at enrollment prior to 29 wks plus 6 days

  • SEVERE pulmonary hypoplasia with US LHR O/E < 25% (measured at 180 to 295 weeks) at the time of surgery

  • Gestational age at FETO procedure 27 weeks 0 days to 29 weeks 6 days as determined by clinical information (LMP) and evaluation of first ultrasound

  • Family meets psychosocial criteria

  • Pre-authorization from third-party payor for fetal intervention OR the ability to self-pay for study treatment. For all patients without insurance or the means to pay for the procedure, an attempt will be made to obtain Medicaid. Insurers that have denied payment have noted that this remains an experimental procedure. As this is a feasibility study and not being offered as either standard of care or as a prospective randomized control trial to determine efficacy, the investigators do not feel that there is a breach of ethical standards.

  • Informed consent

Exclusion Criteria:
  • Failure to meet all inclusion criteria

  • Patient < 18 years of age

  • Multi-fetal pregnancy

  • Rubber latex allergy

  • Preterm labor, cervix shortened (< 15 mm at enrollment or within 24 hours of FETO balloon insertion procedure) or uterine anomaly strongly predisposing to preterm labor, placenta previa

  • Family does not meet psychosocial criteria. Reasons for exclusion include: insufficient social support, inability to understand requirements of the study, inability to reside in or near San Francisco.

  • Right sided CDH or bilateral CDH, isolated left sided with LHR O/E < 25% (measured at 180 to 295 weeks) as determined by ultrasound

  • Additional fetal anomaly by ultrasound, MRI, or echocardiogram at the fetal treatment center. Exclude chromosomal abnormalities, associated anomalies recognized to alter survival prognosis (ie. CDH and congenital heart disease) or presence of an underlying genetic syndrome (ie. Fryns). No cases will be removed post hoc if abnormalities are discovered in the course of post-operative monitoring

  • Maternal contraindication to fetoscopic surgery or severe maternal medical condition in pregnancy

  • History of incompetent cervix with or without cerclage

  • Placental abnormalities (previa, abruption, accrete) known at time of enrollment

  • Maternal-fetal Rh isoimmunization, Kell sensitization or neonatal alloimmune thrombocytopenia affecting the current pregnancy

  • Maternal HIV, Hepatitis-B, Hepatitis-C status positive because of the increased risk of transmission to the fetus during maternal-fetal surgery. If the patient's HIV or Hepatitis status is unknown, the patient must be tested and found to have negative results before enrollment

  • Uterine anomaly such as large or multiple fibroids or mullerian duct abnormality

  • There is no safe or technically feasible fetoscopic approach to balloon placement

  • Participation in another intervention study that influences maternal and fetal morbidity and mortality or participation in this trial in a previous pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of California San Francisco Fetal Treatment Center San Francisco California United States 94158

Sponsors and Collaborators

  • Hanmin Lee

Investigators

  • Principal Investigator: Hanmin Lee, MD, University of California, San Francisco

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Hanmin Lee, Professor, University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT04583644
Other Study ID Numbers:
  • 16-20723
First Posted:
Oct 12, 2020
Last Update Posted:
May 6, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 6, 2022