In Utero Fetoscopic Repair Program for Sacral Myelomeningoceles and Mye-LDM

Not Applicable

Active, not recruiting

• Conditions: Sacral Myelomeningocele; Neural Tube Defects; Spina Bifida
• Interventions: Procedure: Fetoscopy

• Registration Number: NCT04770805
• Lead Sponsor: Assistance Publique - Hôpitaux de Paris

Brief Summary

The purpose of the study is to evaluate the feasibility and the maternal, fetal and postnatal outcomes of sacral myelomeningocele (MMC) and Myelic Limited Dorsal Myeloschisis (MyeLDM) fetoscopic repair at Trousseau Hospital (Paris, France).

Detailed Description

Myelomeningocele and Myelic limited dorsal myeloschisis (MyeLDM) correspond to neural tube defects which lead to lifelong disabilities including lower extremity paralysis, sphincters deficiency, and cerebral complications (Chiari 2 malformation and hydrocephalus). It is demonstrated that fetal surgery repair of MMC with upper limit between the first thoracic vertebra (T1) and the first sacral vertebra (S1) improves motor and cerebral prognosis. Nowadays, this fetal surgery is performed either after maternal laparotomy and hysterotomy (open fetal surgery) or using fetoscopy. the investigators, at Trousseau Hospital (APHP, Paris), initiated an open fetal surgery of MMC program called PRIUM1 and 16 fetuses has been currently operated.

Fetoscopic repair of MMC is proposed by several international groups in order to prevent from maternal and obstetric morbidity related to the hysterotomy and improve the mother's obstetrical prognosis by allowing vaginal delivery. Results of fetoscopic MMC repair are very satisfying, both in terms of repair surgery efficacy and in terms of obstetrical prognosis. The research team believe that it is justified to propose this minimally invasive repair technique using fetoscopy, for represented by sacral MMC (level S1 and lower) as well as for intermediate forms between open and closed dysgraphisms, represented by MyeLDM. Indeed, these dysraphism are associated with the same cerebral complications than MMC with upper limit between T1 and S1 which could be corrected with prenatal repair. In addition, the spinal cord protection offered by prenatal surgery could prevent from the neuroepithelium destruction observed during pregnancy, with a potential motor benefit for the children.

The main objective of PRIUM 2 is to evaluate the success of fetoscopic surgical repair of sacral MMC or MyeLDM with a birth after 32 weeks of gestation and without severe perinatal morbidity and mortality.

The secondary objectives of PRIUM 2 are to evaluate the complications of pregnancy related to fetoscopic surgery as well as to evaluate the prenatal and postnatal evolution of the cerebral complications (Chiari 2 malformation and hydrocephalus) after fetoscopic repair surgery of the dysraphism (up to 12 months of age).

In this protocol, fetal sacral MMC/ MyeLDM repair surgery will be performed using gas fetoscopy before 26 weeks. After an exteriorization of the uterus through a laparotomy, humidified and warmed gas will be insufflated with low pressure (6 to 8mmHg mmHg). Fetoscopic repair surgery will be performed by a multidisciplinary team (maternal fetal medicine specialists, pediatric neurosurgeons, pediatric surgeons).

After discharge, patients will be followed weekly by a midwife and every two weeks by a referring obstetrician who will perform a clinical examination and a fetal ultrasound.A post procedure MRI will be performed 4 weeks after the surgery. If there is no obstetrical contraindication, vaginal delivery will be authorized.

The children will be followed according to the conventional management of children with dysraphisms and consultations at 8 weeks of life and 12 months of life will be scheduled at Trousseau Hospital, with the multidisciplinary team (pediatric neurosurgeons, physical medicine and rehabilitation specialists, pediatric orthopedic surgeons). During these two consultations, the children will have a complete clinical examination, a cerebral and spinal MRI and an ultrasound of the urinary tract.

Study Timeline

• Study First Submitted: 2021-01-24
• Study First Submitted QC: 2021-02-24
• Study First Posted: 2021-02-25
• Study Start: 2021-04-16
• Primary Completion: 2024-11-24
• Status Verified: 2024-12
• Last Update Submitted: 2024-12-26
• Last Update Posted: 2024-12-30
• Study Completion: 2025-12-08

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: Female
• Target Recruitment: 10

Inclusion Criteria

Inclusion Criteria :

• Pregnant women age 18 years and older who are able to consent
• Singleton pregnancy before 26 weeks of gestation,
• Sacral MMC (upper level S1 or below) or MyeLDM diagnosed on ultrasound and MRI, 4. Absence of associated malformation apart from the anomalies usually observed in cases of open dysraphisms (i.e. feet malpositions, associated cerebral signs) or chromosomal anomaly if verification of the karyotype was desired by the couple
• Affiliated to health insurance, understanding and speaking French
• Written consent of the patient for the surgery and representatives of the parental authority for the postnatal follow-up of the child
• Patient who made the choice to continue the pregnancy

Exclusion Criteria

• Abnormal angulation of the fetal spine,
• risk factors for prematurity: cervical length less < 15mm, history of late miscarriage before 22 weeks, pre-existing rupture of the membranes at inclusion,
• Placenta praevia,
• BMI greater than 35 kg / m2,
• Abnormality of the uterus: large fibroid, uterine malformation, history of uterine body surgery
• Maternal infection at risk of maternal-fetal transmission: HIV, HBV, HCV,
• Surgical or anesthetic contraindication.
• Participation in another interventional research protocol,
• Patients under legal protection (guardianship, curatorship).
• Allergies to drugs used in the research

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Fetoscopic repair	Fetoscopy	Sacral Myelomeningocele and Mye-LDM Fetoscopic repair

Primary Outcome Measures

Name	Time	Method
Ability to perform fetoscopic sacral MMC/MyeLDM repair without severe perinatal morbidity and mortality	From time of surgery to 8 weeks of life (up to 28 weeks)	Successful complete closure of the defect using the fetoscopic technique AND birth after 32 weeks without severe perinatal morbidity and mortality including grade III-IV intra ventricular hemorrhage, severe, cerebral parenchyma hemorrhage, periventricular leukomalacia, grade III ulcero-necrotizing enterocolitis, severe bronchodysplasia)

Secondary Outcome Measures

Name	Time	Method
Maternal obstetric outcome as evidenced by antenatal betamethasone treatment	From time of surgery until 34 weeks of gestation	indication for a betamethasone course occuring at any time from surgery until 34 weeks of gestation
Proportion of postpartum hemorrhages	From time of surgery until delivery	Maternal obstetric outcome as evidenced by postpartum hemorrhage Proportion of postpartum hemorrhages defined by blood loss of more than 500mL for vaginal delivery, and 800mL for cesarean delivery
Need for maternal transfusion (number of blood cells transfused)	From time of surgery until delivery	Maternal obstetric outcome as evidenced by postpartum hemorrhage Need for maternal transfusion (number of blood cells transfused)
Adverse early childhood outcome as evidenced by need for a neurosurgical intervention	From the time of birth until 8 weeks of life	need for one of the following neurosurgery; * Type 1: Superficial skin recovery surgery due to scar dehiscence; * Type 2: Need for surgical correction involving all aspects, without reopening the dura; * Type 3: Need for complete surgical correction with repair of the dural plane
Maternal obstetric outcome as evidenced by gestational age at delivery (1)	From time of surgery until delivery	Gestational age of delivery regardless of indication
Adverse neonatal outcome at birth (1)	at birth	Normal or abnormal birth parameters at birth depending on the term
Maternal obstetric outcome as evidenced by preterm labor leading to delivery at less than 37 weeks of gestation	From time of surgery until 37 weeks of gestation	Preterm labor occuring at any time from surgery leading to delivery before 37 weeks of gestation
Maternal obstetric outcome as evidenced by chorioamnionitis	From time of surgery until 37 weeks of gestation	chorioamnionitis occuring at any time from surgery until 37 weeks of gestation
Maternal obstetric outcome as evidenced by the ability to deliver vaginally	From time of surgery until delivery	Mode of delivery - either vaginal or cesarean section
Postnatal evolution of brain abnormalities associated with open dysraphism (3)	From the time of birth until 12 months of life	Proportion of patients requiring a cerebrospinal fluid shunt within the first 12 months of life
Other Maternal obstetric outcome as evidenced by hypertensive disorders, preeclampsia, gestational diabetes	From time of surgery until 37 weeks of gestation	hypertensive disorders, preeclampsia, gestational diabetes occuring any time from surgery until 37 weeks of gestation
Adverse neonatal outcome at birth (2)	at birth	Proportion of fetal asphyxia (arterial pH at the umbilical cord \<7.00)
Postnatal evolution of brain abnormalities associated with open dysraphism	From the time of birth until 12 months of life	Difference in the growth of the cephalic perimeter by measuring the cranial perimeter between birth and the age of 12 months
Adverse Maternal outcome	during the surgery	diagnosis of maternal gas embolism, hemorrhage, thromboembolic complication, death
Maternal obstetric outcome as evidenced by preterm premature rupture of membranes	From time of surgery until 37 weeks of gestation	Preterm premature rupture of membranes occuring at any time from surgery until 37 weeks of gestation
Prenatal evolution of brain abnormalities associated with open dysraphism, after fetoscopic repair	From time of surgery until birth	Difference in the growth of the cephalic perimeter measured on an axial ultrasound section
Prenatal evolution of brain abnormalities associated with open dysraphism, after fetoscopic repair (1)	From time of surgery until birth	Difference in measurement of the ventricles on an axial ultrasound section
Prenatal evolution of brain abnormalities associated with open dysraphism, after fetoscopic repair (2)	From time of surgery until birth	Difference in the measurement of the large retro-cerebellar cistern on an axial section of the posterior fossa
Prenatal evolution of brain abnormalities associated with open dysraphism, after fetoscopic repair (3)	From time of surgery until birth	Proportion of patients with reversal of hindbrain herniation (i.e. lower limit of the vermis located above the foramen magnum on ultrasound and/or fetal MRI)
Maternal obstetric outcome as evidenced by gestational age at delivery (2)	From time of surgery until delivery	Proportion of deliveries before 37 weeks of gestation
Postnatal evolution of brain abnormalities associated with open dysraphism (1)	From the time of birth until 12 months of life	Difference in the measurement of the cerebral lateral ventricles measured during postnatal transfrontanellar ultrasound followed by cerebral MRI ,
Postnatal evolution of brain abnormalities associated with open dysraphism (2)	From the time of birth until 12 months of life	Proportion of patients with reversal of hindbrain herniation (i.e. lower limit of the vermis located above the foramen magnum on cerebral MRI)

Trial Locations

Locations (1)

Service médecine foetale-Hôpital Trousseau; 🇫🇷 Paris, France