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Feto-Endoscopic Tracheal Occlusion (FETO) for Severe Congenital Diaphragmatic Hernia

Children's Hospital Medical Center, Cincinnati · NCT02986087

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–50 · Women only
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
40
US sites recruiting
1
Study start
November 2016
Record last updated
May 11, 2025

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

Tracheal occlusion IDE approved by FDA for congenital diaphragmatic hernia fetuses.

Being studied: Fetal Tracheal Occlusion

Conditions: Congenital Diaphragmatic Hernia; Pulmonary Hypoplasia; Pulmonary; Hypertension

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Isolated CDH with liver up
  • Severe pulmonary hypoplasia with ultrasound O/E LHR \<25% at the time of surgery
  • Gestational age at FETO procedure 27 weeks 0 days to 29 weeks 6 days
  • Moderate pulmonary hypoplasia with ultrasound O/E LHR \<30% and liver-up at the time of surgery
  • Gestational age at FETO procedure 30 weeks 0 days to 31 weeks 6 days in this moderate category
  • Maternal age greater than or equal to 18 years
  • Gestational age at enrollment prior to 29 weeks 6 days, or 31 weeks 6 days in moderate category
  • Normal karyotype or FISH
  • Normal fetal echocardiogram
  • Singleton pregnancy
  • Willing to remain in the greater Cincinnati area for remainder of pregnancy
  • Family considered and decline option of termination of the pregnancy at less than 24 weeks 0 days
  • Family meets psychosocial criteria

Exclusion Criteria

  • Patient \< 18 years old
  • Multi-fetal pregnancy
  • Rubber latex allergy
  • Preterm labor, cervix shortened (\<15 mm) or uterine anomaly strongly predisposing to preterm labor, placenta previa
  • Bilateral CDH, isolated left sided CDH with an O/E > 30%
  • Additional fetal anomaly by ultrasound, MRI, or echocardiogram
  • Chromosomal abnormalities
  • Maternal contraindications to fetoscopic surgery or severe maternal condition in pregnancy
  • Incompetent cervix with or without a cerclage
  • Placental abnormalities known at time of enrollment
  • Maternal HIV, Hepatits B, Hepatitis C
  • Maternal uterine anomaly
  • 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

Recruiting US locations

  • Cincinnati Children's Hospital Medical Center (CCHMC)

    Cincinnati, OH 45229

    Site contact: Foong-Yen Lim, MD · 513-803-5270 · Foong.Yen.Lim@cchmc.org

Study contacts (from the official record)

  • Foong-Yen Lim, MD · (513) 636-6259 · Foong-Yen.Lim@cchmc.org
  • Jose Peiro, MD, PhD · (513) 803-4563 · Jose.Peiro@cchmc.org
Feto-Endoscopic Tracheal Occlusion (FETO) for Severe Congenital… (NCT02986087) | Bored Studies