Status:
COMPLETED
Fetoscopic Meningomyelocele Repair Study
Lead Sponsor:
Baylor College of Medicine
Conditions:
Neural Tube Defect
Eligibility:
FEMALE
18-64 years
Phase:
PHASE1
Brief Summary
The purpose of the study is to evaluate the maternal and fetal outcomes of a new technique for the fetoscopic repair of fetal MMC at Texas Children's Hospital Pavilion for Women. The investigators hy...
Detailed Description
Spina bifida can be a devastating neurological congenital anomaly . It results from incomplete closure of the neural tube between 22 and 28 embryological days. Its incidence is approximately 1-2 per 1...
Eligibility Criteria
Inclusion
- Pregnant women - maternal age 18 years or older and capable of consenting for their own participation in this study,
- Singleton pregnancy,
- MMC with the upper boundary located between T1 and S1,
- Evidence of hindbrain herniation (confirmed on MRI to have an Arnold-Chiari type II malformation),
- Absence of chromosomal abnormalities and associated anomalies,
- Gestational age at the time of the procedure will be between 19 0/7 weeks and 25 6/7 weeks,
- Normal karyotype and/or normal chromosomal microarray (CMA) by invasive testing (amniocentesis or CVS). If there is a balanced translocation with normal MCA with no other anomalies the candidate can be included. Patients declining invasive testing will be excluded.
- Family has considered and declined the option of termination of the pregnancy at less than 24 weeks,
- Family meets psychosocial criteria (sufficient social support, ability to understand requirements of the study), and
- Parental/guardian permission (informed consent) for follow up of child after birth.
Exclusion
- Fetal anomaly unrelated to MMC,
- Severe kyphosis,
- Increased risk for preterm labor including short cervical length (\<1.5 cm), history of incompetent cervix with or without cerclage, and previous preterm birth,
- Placental abnormalities (previa, abruption, accreta) known at time of enrollment,
- A pre-pregnancy body-mass index ≥40,
- Contraindications to surgery including previous hysterotomy (whether from a previous classical cesarean, uterine anomaly such as an arcuate or bicornuate uterus, major myomectomy resection, or previous fetal surgery) in active uterine segment,
- Technical limitations precluding fetoscopic surgery, such as uterine fibroids, fetal membrane separation, and uterine anomalies,
- 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,
- Maternal medical condition that is a contraindication to surgery or anesthesia,
- Low amniotic fluid volume (Amniotic Fluid Index less than 6cm) if deemed to be due to fetal anomaly, poor placental perfusion or function, or membrane rupture. Low amniotic fluid volume that responds to maternal hydration is not an exclusion criterion,
- Patient does not have a support person (e.g. Spouse, partner, mother) available to support the patient for the duration of the pregnancy,
- Inability to comply with the travel and follow-up requirements of the trial,
- Participation in another intervention study that influences maternal and fetal morbidity and mortality or participation in this trial in a previous pregnancy, and
- Patient scores as severely depressed on the BDI-II questionnaire; a score of 29 or above.
- Maternal hypersensitivity to collagen.
Key Trial Info
Start Date :
July 29 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 23 2025
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT02230072
Start Date
July 29 2014
End Date
June 23 2025
Last Update
July 10 2025
Active Locations (2)
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1
Stanford University: Lucille Packard's Childrens Hospital
Stanford, California, United States, 94305
2
Texas Childrens Hospital
Houston, Texas, United States, 77030