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Syndrome clinical trials

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NCT ID: NCT02108119 Completed - Clinical trials for Irritable Bowel Syndrome

The Effect of Probiotics on Symptoms and Intestinal Flora in Patients With Irritable Bowel Syndrome

Start date: May 2, 2014
Phase: Phase 2
Study type: Interventional

To demonstrate benefit of a probiotic product in adults with irritable bowel syndrome.

NCT ID: NCT02107196 Completed - Clinical trials for Irritable Bowel Syndrome With Diarrhea

12-Week Efficacy and Safety Study of Ibodutant in Women With Irritable Bowel Syndrome With Diarrhea (IBS-D)

IRIS-3
Start date: March 2014
Phase: Phase 3
Study type: Interventional

Irritable Bowel Syndrome with diarrhoea (IBS-D) is a functional gastrointestinal disorder characterised by chronic or recurrent abdominal pain or discomfort and diarrhoea. This trial aims at the evaluation of the efficacy and safety of oral ibodutant 10 mg once daily as compared to placebo in women with IBS-D over a 12-week treatment period.

NCT ID: NCT02106637 Recruiting - Smoking Cessation Clinical Trials

Early In-hospital Initiation of Pharmacotherapy for Smoking Cessation, Patients After ACS

Start date: October 2016
Phase: N/A
Study type: Interventional

The hypothesis of this study is that combination of Varenicline treatment with nurse-led hospital support during hospitalization and after discharge will result in clinically significant higher long term abstinence rates in smokers with ACS, as compared with nurse led support and placebo, without a significant increase in the risk of adverse events.

NCT ID: NCT02105428 Completed - Overweight Clinical Trials

Potential Impact of Polycystic Ovarian Syndrome on Protein Modifications and Accumulation

Start date: July 2010
Phase: N/A
Study type: Interventional

A goal of this study is to use a novel methodology to determine whether insulin resistance in women with polycystic ovary syndrome (PCOS) is related to the accumulation of proteins with modifications. This could lead to future research to determine if these modifications interfere with their proper function. Additionally, the investigators will determine how protein quality is affected by exercise training. Aerobic exercise enhances the endogenous oxidant buffering systems which may minimize oxidative damage to proteins. The investigators propose that aerobic exercise minimizes the accrual of modified proteins by increasing the synthesis of new proteins, but also by increasing the degradation and removal of old and damaged proteins. Based on our previous studies the investigators observed that insulin affects plasma protein synthesis and aerobic exercise improves insulin sensitivity not only in muscle but also in liver. The investigators therefore propose that aerobic exercise and related increase in insulin sensitivity (and decline in insulin levels) will reduce accumulation of old and modified skeletal muscle and plasma proteins leading to improved function.

NCT ID: NCT02104336 Terminated - Pearson Syndrome Clinical Trials

Phase 2 Study of EPI-743 in Children With Pearson Syndrome

Start date: August 31, 2014
Phase: Phase 2
Study type: Interventional

Treatment of Pediatric Subjects with Pearson syndrome

NCT ID: NCT02103478 Completed - Clinical trials for Myelodysplastic Syndrome

Pharmacokinetic Guided Dose Escalation and Dose Confirmation With Oral Decitabine and Oral Cytidine Deaminase Inhibitor (CDAi) in Patients With Myelodysplastic Syndromes (MDS)

Start date: October 28, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This first-in-human, 3-stage, open-label study evaluated the safety and pharmacokinetics of ASTX727, as well as determined the dose for later stages.

NCT ID: NCT02103140 Active, not recruiting - Obesity Clinical Trials

An Exercise RCT Targeting African-American Women With Metabolic Syndrome and High Risk for Breast Cancer

Start date: January 2012
Phase: N/A
Study type: Interventional

Among African-American women, in whom metabolic syndrome (MetS) is very prevalent and breast cancer mortality rates are high, it is hypothesized that intervening on MetS to improve the MetS profile may prove to be a means to reduce breast cancer risk. Specific recommendations for breast cancer prevention are now focused on maintaining a healthy weight via increased physical activity levels, and losing weight if overweight or obese. This pilot project compares two exercise interventions: a supervised facility-based and a home-based exercise intervention to a control group in African-American women with metabolic syndrome who are at high risk for breast cancer. This study is a 6-month three-arm RCT to assess the impact of the exercise interventions on biomarkers related to obesity, insulin-related pathways, inflammation, hormones, and micro-RNAs. The specific aim of the proposed study is to compare the impact of a supervised facility-based and a home-based exercise intervention on obesity, metabolic syndrome and known breast cancer biomarkers in postmenopausal African-American women with metabolic syndrome who are at increased risk of breast cancer.

NCT ID: NCT02102698 Completed - Tourette's Syndrome Clinical Trials

Ecopipam Treatment of Tourette's Syndrome in Subjects 7-17 Years

Start date: March 2014
Phase: Phase 2
Study type: Interventional

Tourette's Syndrome is a neurological disease characterized by motor and vocal tics. It has been hypothesized that abnormal interactions of dopamine with its receptors may cause the tics. The purpose of this study is to test the hypothesis that a drug (ecopipam) that selectively blocks dopamine D1/D5 receptors can reduce the frequency and severity of the tics.

NCT ID: NCT02101138 Active, not recruiting - Clinical trials for Hypereosinophilic Syndrome

Study to Evaluate Safety and Efficacy of Dexpramipexole (KNS-760704) in Subjects With Hypereosinophilic Syndrome

Start date: March 14, 2014
Phase: Phase 2
Study type: Interventional

Background: - Eosinophils are white blood cells that fight infections. In people with hypereosinophilic syndrome (HES), eosinophil levels are too high and can damage their organs. HES is usually treated with steroids, but steroids can cause side effects and stop working over time. Researchers want to see if a drug called dexpramipexole, being developed by Knopp Pharmaceuticals, can help people with HES to reduce their steroid dose. Objective: - To test whether dexpramipexole can reduce the steroid dose needed to control eosinophilia and HES symptoms. Eligibility: - Adults 18 and older with HES who respond to steroids, but need more than 10 mg daily to control eosinophilia and symptoms. Design: - The study will last 9 months with 6 visits to NIH. - Participants will be screened with medical history, physical exam, and urine and blood samples. - Participants steroids will be tapered to the lowest effective dose. During this time, blood will be drawn weekly. Participants will take this dose for 2 weeks before starting the study drug. - Participants will take the study drug twice daily by mouth for 12 weeks along with steroids. The steroid dose will not be decreased during this time and participants will be seen monthly for a medical history, physical examination and blood work. - Just before and 12 weeks after starting the study drug, the following tests will be performed: - medical history and physical exam - blood and urine tests - lung function tests - electrocardiogram (measures heart electrical activity) - echocardiogram (takes pictures of the heart using sound waves) - bone marrow biopsy (a needle inserted into the hip bone that removes bone marrow cells for study) - After 12 weeks, the participants steroid dose will be tapered again to the lowest effective dose while on study drug. - Two weeks after the lowest effective dose is reached, participants will return for a medical history, physical examination, blood work, lung and heart tests. - Participants who respond to the study drug may be able to continue to receive the drug on a planned separate study. - Four weeks after stopping the study drug, participants will have medical history, physical exam, and blood tests.

NCT ID: NCT02100371 Completed - Clinical trials for Basal Cell Nevus Syndrome

Study of BMS-833923 in Two Specific Patients With Basal Cell Nevus Syndrome

Start date: February 2014
Phase: N/A
Study type: Interventional

This is an extension study of Protocol CA194002 to allow 2 specific participants with basal cell nevus syndrome in the CA194002 study at Princess Margaret Cancer Centre who are still benefitting from the study drug BMS-833923 to continue receiving the study drug. This study will continue to evaluate the safety and tolerability of BMS-833923 in these participants.