Cincinnati, OHNCT02986087Now EnrollingIRB Ready

Congenital Diaphragmatic Hernia Clinical Trial in Cincinnati, OH

Access cutting-edge congenital diaphragmatic hernia treatment through this clinical trial at a research site in Cincinnati. Study-provided care at no cost to qualified participants.

Sponsored by Children's Hospital Medical Center, Cincinnati

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Expert Care in Cincinnati

Access congenital diaphragmatic hernia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related congenital diaphragmatic hernia treatment provided free

Apply for This Cincinnati Location

Check if you qualify for this congenital diaphragmatic hernia clinical trial in Cincinnati, OH

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Cincinnati

    Convenient for OH residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Cincinnati site if eligible
  4. 4Begin participation

About This Congenital Diaphragmatic Hernia Study in Cincinnati

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

Sponsor: Children's Hospital Medical Center, Cincinnati

Who Can Participate

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

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Cincinnati?

Yes, this clinical trial (NCT02986087) has an active research site in Cincinnati, OH that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Congenital Diaphragmatic Hernia Treatment Options in Cincinnati, OH

If you're searching for congenital diaphragmatic hernia treatment options in Cincinnati, OH, this clinical trial (NCT02986087) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Cincinnati research site is actively enrolling participants for this clinical trial. You'll receive care from experienced congenital diaphragmatic hernia specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all congenital diaphragmatic hernia clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Cincinnati, OH