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Spinal Dysraphism clinical trials

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NCT ID: NCT01096459 Withdrawn - Spina Bifida Clinical Trials

Nerve Rerouting Treatment for Neurogenic Bladder in Spina Bifida

Start date: January 2013
Phase: N/A
Study type: Interventional

The goal of this study is to evaluate a surgical procedure (operation) that reroutes lumbar to sacral nerves in the spinal column to improve the bladder's ability to empty properly in patients born with Spina Bifida.

NCT ID: NCT00767988 Withdrawn - Clinical trials for Urinary Tract Infection

Probiotics in Girls With Spina Bifida

Start date: n/a
Phase: Phase 2
Study type: Interventional

Girls with spina bifida also have bladder problems. This is because they need temporary placement of a tube into the bladder to remove urine. This thin flexible tube is called a catheter. It can increase the risk of having bacteria in the urine. This in turn can lead to urinary tract infection (UTI). Some girls with spina bifida are given antibiotics. These are medicines used to treat infections caused by bacteria. The medicine is used to prevent UTI. However, long-term treatment with these medicines can have side effects. For example, the bacteria may become resistant to the antibiotics. Also, bacteria in the urine can persist. UTI can still occur in patients on antibiotics. UTI in girls occurs because bacteria migrate from the rectum to the vagina area. This gives the bacteria access to the bladder. Also, in girls with spina bifida, the access to the bladder is easier because of the catheter. Probiotics are friendly bacteria. They are available as dietary supplements and as food. They contain helpful bacteria. Yogurt is an example of a food that contains probiotics. The purpose of this study is to find out, if probiotics taken for 6 months can prevent UTI in girls with spina bifida. We will also try to find out whether changes in urine bacteria are associated with the taking of the probiotics. A vaginal and rectal swab will also be done to find out if taking probiotics has any benefits on preventing bacteria.

NCT ID: NCT00301587 Withdrawn - Neural Tube Defects Clinical Trials

A Study to Evaluate Folate Levels in Women Taking Oral Contraceptives

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare red blood cell folate levels in women who are taking oral contraceptives with or without folic acid