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Neural Tube Defects clinical trials

View clinical trials related to Neural Tube Defects.

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NCT ID: NCT05962086 Recruiting - Spinal Dysraphism Clinical Trials

Determining Developmental and Clinical Markers Affecting Urinary Function of Children With Spinal Dysraphism

Start date: October 22, 2022
Phase:
Study type: Observational

To identify developmental and clinical biomarkers that affect urinary incontinence at the ages of 5, 7, and 10 according to different neuro-urological clinical factors.

NCT ID: NCT05718440 Recruiting - Spinal Dysraphism Clinical Trials

Uronephrological Complications Risk Factors in Spinal Dysraphism

RUD
Start date: November 6, 2023
Phase:
Study type: Observational

Spinal dysraphism consist of congenital malformations resulting of abnormalities in the formation of neural tube and/or surrounding structures during embryogenesis. The aim of this study is to assess if there are specific clinical and paraclinical patterns of pelvic (urinary, bowel, sexual) disorders depending on the dysraphism's type and level of injury. This description will help to determine a prognosis on symptoms and the risk of complication depending on the dysraphism's type and level of injury. It will provide targeted evaluation and cares: identifying patients who will be at risk of complications and needing acute monitoring or preventing cares on the symptoms' onset. Pelvic disorders have an important impact on morbi-mortality (urinary dysfunction is the first cause of mortality in adults by renal failure or infection) and also on patients' quality of life.

NCT ID: NCT05672849 Recruiting - Neural Tube Defects Clinical Trials

Safety and Efficacy of Devices Used in Fetoscopic Neural Tube Defect Repair Cases

Start date: November 14, 2022
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the safety and efficacy of devices used in patients undergoing fetoscopic neural tube defect repair.

NCT ID: NCT05163899 Recruiting - Clinical trials for Tethered Cord Syndrome

Investigation of Surgical Sectioning of the Filum Terminale in Treating Occult Tethered Cord Syndrome Patients

OCCULT
Start date: May 19, 2022
Phase: Phase 2
Study type: Interventional

The investigators hypothesize that surgical release of the filum terminale (strand of fibrous tissue at the end of the spinal cord) is a more efficacious treatment option for symptomatic relief than medical management in subjects with Occult Tethered Cord Syndrome (OTCS) and that the risks do not outweigh the benefit profile.

NCT ID: NCT04770805 Recruiting - Spina Bifida Clinical Trials

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

PRIUM2
Start date: April 16, 2021
Phase: N/A
Study type: Interventional

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).

NCT ID: NCT04738539 Recruiting - Urologic Diseases Clinical Trials

Efficacy of Contrast Enhanced Voiding Urosonography for Urodynamic Studies

Start date: March 2, 2021
Phase:
Study type: Observational

The investigators will assess the feasibility of replacing fluoroscopy/iodinated contrast with ultrasound/sulfur hexafluoride lipid-type A microspheres during routine urodynamic studies.

NCT ID: NCT04523233 Recruiting - Neural Tube Defects Clinical Trials

Metals/Vitamins Levels in NTD

NTD&HMs
Start date: August 25, 2020
Phase:
Study type: Observational

Introduction: Heavy metals important pollutants produced from anthropogenic activities, has been suggested to be embryotoxic and fetotoxic in a lot of studies. The aims of this study were to determine the levels of trace elements and heavy metals, namely folic acid, zinc (Zn), molybdenum (Mo), vanadium (V), strontium (Sr), aluminium (Al), tin (Sn), antimony (Sb), mercury (Hg), calcium (Ca), iron ( Fe), magnesium (Mg), phosphorus (P), barium (B) and selenium (Se), in the amniotic fluid of pregnant women, and to investigate their relationship with neural tube defects (NTDs). Methods: The study will be included 70 pregnant women whose fetuses were complicated with NTDs (study group) and 70 pregnant women with unaffected healthy fetuses (control group). The samples levels of elements and vitamins will be measured using inductively coupled plasma-mass spectrometry and will be compared between the two groups.

NCT ID: NCT04362592 Recruiting - Spina Bifida Clinical Trials

In-Utero Endoscopic Correction of Spina Bifida

Start date: November 2, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the feasibility and effectiveness of performing fetoscopic surgical correction of fetal spina bifida. Two surgical approaches will be utilized: the percutaneous technique versus the laparotomy/uterine exteriorization technique.

NCT ID: NCT03856034 Recruiting - Spina Bifida Clinical Trials

Laparotomy Versus Percutaneous Endoscopic Correction of Myelomeningocele

Start date: November 2, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the feasibility of a fetoscopic surgical technique for antenatal correction of fetal myelomeningocele. Two surgical approaches will be utilized. The percutaneous approach will be offered to participants with a posterior placenta. The laparotomy/uterine exteriorization approach will be offered to participants regardless of placental location.

NCT ID: NCT03315637 Recruiting - Hydrocephalus Clinical Trials

Fetal Endoscopic Surgery for Spina Bifida

FESSB
Start date: January 2015
Phase: N/A
Study type: Interventional

This study aims to assess the feasibility to perform a fetoscopic prenatal repair of an open neural tube defect, and secondly to assess the maternal, fetal and neonatal outcomes.