Clinical Trials Logo

Meningocele clinical trials

View clinical trials related to Meningocele.

Filter by:
  • None
  • Page 1

NCT ID: NCT05188300 Completed - Meningomyelocele Clinical Trials

Propellers Flaps for Meningomylocele Defects

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

To evaluate reliability of free style propeller perforator flap for coverage MMC soft tissue defect follow a well-established step that overcome the usual problem of pedicled perforators propellers flaps.

NCT ID: NCT05033275 Recruiting - Clinical trials for Infant of Diabetic Mother

Screening for Sacral Agenesis in Offspring of Mothers With Diabetes in Pregnancy

Start date: May 1, 2021
Phase:
Study type: Observational

Babies born to mothers with pregestational diabetes will be screened with parental consent for sacral agenesis

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: NCT01793168 Recruiting - Clinical trials for Retinitis Pigmentosa

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

CoRDS
Start date: July 2010
Phase:
Study type: Observational [Patient Registry]

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access. Visit sanfordresearch.org/CoRDS to enroll.