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| ID | Type | Description | Link |
|---|---|---|---|
| 1R01HD119340-01 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) | NIH |
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The objective is to test the efficacy of a laparotomy-assisted fetoscopic surgical approach to cover spina bifida spinal cord developmental defects using cryopreserved human umbilical cords (NEOX Cord 1K®) as a meningeal and skin patch.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NEOX Cord 1K applied fetoscopically | Experimental | Patients intending to undergo open in-utero spina bifida repair will be offered to be screened for an alternative minimally invasive approach. All eligible pregnant mothers' fetuses within the trial will receive NEOX Cord 1K® as a spinal cord cover to close the developmental defect. In some cases, at the discretion of the Pediatric Neurosurgeon, NEOX Cord 1K® may be required to cover the skin. All eligible subjects meeting all inclusion criteria but none of the exclusion criteria may be enrolled. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| NEOX Cord 1K applied fetoscopically | Device | Under general anesthesia and tocolysis, in-utero repair begins with a laparotomy that is followed by exteriorization of the uterus. The fetus is then positioned by external cephalic version. Uterine entry will be accessed using 3 cannulas, followed by heated-humidified carbon dioxide insufflation for visualization. Then, fetoscopically the placode will be examined and dissected. The lesion will be repaired using NEOX Cord 1K® (HUC) for closure of the first layer over the neural placode. Primary closure of the skin will then occur, or NEOX Cord 1K® (human umbilical cord) will be used for skin closure at the discretion of the Pediatric Neurosurgeon. Finally, the laparotomy site will be sutured in multiple layers. |
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants that can ambulate independently by walking at least 10 steps | 30-36 months after delivery |
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with lower extremity motor and sensory levels exceeding the anatomical level of the lesion by ≥ 2 segments | 30-36 months after delivery |
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Inclusion Criteria:
Maternal Inclusion Criteria:
Fetal Inclusion Criteria:
Exclusion Criteria:
Maternal Exclusion Criteria:
Fetal exclusion criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Ramesha Papanna, MD, MPH | Contact | (713) 500-6423 | Ramesha.Papanna@uth.tmc.edu | |
| Stephanie W Conaway, BSN | Contact | (713) 486-6558 | Stephanie.L.Whitney@uth.tmc.edu |
| Name | Affiliation | Role |
|---|---|---|
| Ramesha Papanna, MD, MPH | The University of Texas Health Science Center, Houston | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The University of Texas Health Science Center at Houston | Recruiting | Houston | Texas | 77030 | United States |
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| ID | Term |
|---|---|
| D016135 | Spinal Dysraphism |
| D008591 | Meningomyelocele |
| ID | Term |
|---|---|
| D009436 | Neural Tube Defects |
| D009421 | Nervous System Malformations |
| D009422 | Nervous System Diseases |
| D000013 | Congenital Abnormalities |
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| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |