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Meningomyelocele clinical trials

View clinical trials related to Meningomyelocele.

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NCT ID: NCT03061084 Recruiting - Spina Bifida Clinical Trials

Prospective Cohort of Transitional Urology Patients

Start date: August 27, 2015
Phase:
Study type: Observational

A transitional Urology database was created in parallel with National Spina Bifida registry to follow patients with complex congenital urogenital anomalies and be able to prospectively evaluate them. The investigators obtained the standardized questionnaires to collect long-term data regarding patients' genitourinary status including urine and fecal continence, sexuality, fertility, and pelvic health.

NCT ID: NCT03044821 Terminated - Neural Tube Defect Clinical Trials

Open Myelomeningocele Repair With High Maternal BMI

Start date: July 18, 2018
Phase: N/A
Study type: Interventional

Spina bifida is a neurological abnormality characterized by an opening in the skin and exposure of the spinal cord on the back of the baby at the time of birth. The complete closure and separation of the spinal cord from the skin occurs in the first month of pregnancy. This form of spina bifida is associated with leg weakness, sensation loss, and bowel and bladder incontinence. The majority of patients (>80%) also develop increased fluid in the brain, called hydrocephalus, and require additional surgery to treat this problem. Standard treatment of myelomeningocele (MMC) involves closing the opening in the back within the first 3 days of life. The surgery releases the spinal cord from the skin and brings the skin edges together to prevent infection and injury to the exposed nerves. Of note, this type of surgery does not improve function. The investigators want to study the open in-utero fetal surgery technique in patients who are candidates for the standard open fetal repair technique but have a pre-pregnancy BMI of 35.0-40.0. The latter is a reason for exclusion for open fetal repair in most centers in the United States.

NCT ID: NCT02664207 Completed - Obesity Clinical Trials

Extended Criteria For Fetal Myelomeningocele Repair

Start date: January 26, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to offer pre-natal Myelomeningocele (MMC) repair surgery to pregnant women with one of the former surgery exclusion factors - A BMI of 35-40 kg/m2 - Diabetes; patients will require good glycemic control - History a previous preterm birth, as long as it was followed by a full term birth - Structural abnormality in the fetus; abnormality must be minor, not increasing the risk of prematurity. For example cleft lip and palate, minor ventricular septal defect, pyelectasis. - Maternal Rh alloimmunization. Must have a low level of anti-red blood cell antibody that is not associated with fetal disease, specifically anti-E < 1:4 or anti-M. Or alloimmunization with negative fetal red blood cell antigen status determined by amniocentesis. We will be extending the Management of Myelomeningocele Study (MOMs) criteria by including these factors. Prenatal clinical and outcome information will be collected; safety and efficacy will be evaluated

NCT ID: NCT02595411 Completed - Stroke Clinical Trials

Reliability of the Melbourne Assessment

Start date: July 2015
Phase: N/A
Study type: Observational

The aim of the study is to investigate the reliability of the Melbourne Assessment.

NCT ID: NCT02509377 Terminated - Pregnancy Clinical Trials

Fetal Myelomeningocele Repair With Maternal BMI Between 35.0 and 40.0

MOMSto40BMI
Start date: July 2015
Phase: N/A
Study type: Interventional

Inclusion and exclusion criteria for fetal repair of MMC was established by the Management of Myelomeningocele Study (MOMS Trial) and these criteria are the standard of care throughout the United States. These criteria state exclusion for hypertension and diabetes which are known co-morbidities for obesity. Investigators plan to expand one exclusion criteria for open fetal repair surgery. Currently, an exclusion factor is a maternal BMI of 35.0 and greater.Investigators will maintain all other inclusion and exclusion criteria (including excluding for hypertension and diabetes) with the exception of expanding the BMI to include mothers with a BMI of 35.0 to 40.0. Co-morbidities of the research group will be compared to the comorbidities of the mothers published in the MOMS trial.

NCT ID: NCT02493062 Terminated - Pregnancy Clinical Trials

Evaluation of Hysterotomy Site After Open Fetal Surgery

Hysterotomy
Start date: June 2013
Phase: N/A
Study type: Interventional

This study is to review how the uterus heals after having open fetal surgery. Open fetal surgery causes a scar perhaps two: one from the open fetal surgery and a second from delivery by cesarean section; rarely, the same area of your uterus was used for both open fetal surgery and delivery. From other studies of surgery performed on a uterus, some of the uterine scars do not heal well. This study's intervention uses sterile saline to spread open the inside of the uterus. The saline is slowly injected into the uterus using a catheter. An ultrasound called a sonohysterogram is performed to take pictures of the uterus, its inside and the walls of the uterus. In this way, the healed areas from the uterine surgery can be seen with ultrasound and evaluated. This is performed at least 6 months after delivery. Primary Outcome: Measure the depth of the scar and location of the scar 6 months or longer after delivery.

NCT ID: NCT02390895 Completed - Myelomeningocele Clinical Trials

Prenatal Endoscopic Repair of Fetal Spina Bifida

ENDOSPIN
Start date: May 17, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the feasibility of prenatal minimally-invasive fetoscopic closure with i) uterine exteriorization for a minimally-invasive repair under amniotic carbon dioxide insufflation ii) two trocars for the dissection and the cover with one patch or the suture of the skin edges by stitch

NCT ID: NCT02368223 Completed - Stroke Clinical Trials

Feasibility of the Portable YouGrabber System

YouGrabber
Start date: October 2014
Phase: N/A
Study type: Interventional

The aim of the study is to determine the feasibility of the portable version of the YouGrabber® system in children with central motor disorders.

NCT ID: NCT02227407 Recruiting - Spinal Cord Injury Clinical Trials

Reciprocating Gait Orthoses for Paraplegia Patients

UPGO
Start date: August 2013
Phase: N/A
Study type: Interventional

Ambulation would bring many physiological and psychological benefits and getting up and walking has been a dream for paraplegia patients.The reciprocating gait orthoses (RGOs) for paraplegics particularly draws research attentions because it mimics human gait pattern.But, the high energy consumption and low walking speeds caused the frequent abandonment or the low utilization of the reciprocating gait orthoses.To improve the design reducing the energy expenditure, it requires biomechanical analysis of the pathological gait such that the gait deviations and energy consuming mechanisms can be identified and remedial means can be implemented. The investigators hypotheses will include that there would exist an energy saving mechanism of human reciprocating locomotion based on the principle of conservation of mechanical energy.Secondly, kinematic and kinetic gait determinants could be derived from the energy saving mechanism. Finally, the control of knee joint coordinating with the hip joint movements would facilitate the gait progression and further reduce the energy consumption. The objective of this clinical trial is to evaluate the gait of paraplegic patients with reciprocating gait orthoses and to support the investigators research in biomechanical analysis, design and control of reciprocating gait orthoses for paraplegia patients. An experiment to study the pathological gait of paraplegia patients with an existing reciprocating gait orthosis will be carried out.

NCT ID: NCT01983345 Completed - Clinical trials for Foetus With Myelomeningocele

Prenatal Surgical Repair of Fetal Myelomeningocele

PRIUM
Start date: July 10, 2014
Phase: N/A
Study type: Interventional

The open surgical repair of myelomeningoceles before 26 weeks gestational age provides a correction of the anomaly of Chiarri, reduces the incidence of ventriculomegaly (defined as a measure of the ventricles at the crossroads ≥ 10 mm), and get a lower of injury than one corresponding to the anatomical defect (as defined by the last upper normal vertebra before the defect). The purpose of this study is to introduce in France an innovative technique for prenatal repair of myelomeningocele until now developed only on the American continent.