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NCT02986087Recruiting

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

Source: ClinicalTrials.gov · Last updated 11 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
6 Dec 2016
Start date
Nov 2016
Primary completion date
Dec 2025
Lead sponsor
Children's Hospital Medical Center, Cincinnati
NCT number
NCT02986087

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From Nov 2016 to the primary completion date, Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

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

Other illness

  • Rubber latex allergy
  • Maternal contraindications to fetoscopic surgery or severe maternal condition in pregnancy
  • Maternal HIV, Hepatits B, Hepatitis C

Age

  • Patient \< 18 years old

Other

  • Multi-fetal pregnancy
  • 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
  • Incompetent cervix with or without a cerclage
  • Placental abnormalities known at time of enrollment
  • Maternal uterine anomaly
  • No safe or technically feasible fetoscopic approach to balloon placement

Who the study is looking for

  • 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

Age in the registry: 18 years to 50 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Cincinnati Children's Hospital Medical Center (CCHMC)
Coordinator of this site? Confirm its status
CincinnatiUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.