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Syndrome clinical trials

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NCT ID: NCT02658487 Active, not recruiting - Clinical trials for Acute Myeloid Leukemia

Vosaroxin and Infusional Cytarabine in Treating Patients With Untreated Acute Myeloid Leukemia

VITAL
Start date: March 2016
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well vosaroxin and cytarabine work in treating patients with untreated acute myeloid leukemia. Drugs used in chemotherapy, such as vosaroxin and cytarabine, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.

NCT ID: NCT02658188 Completed - Clinical trials for Restless Legs Syndrome

Long-term Efficacy and Safety of Gabapentin Enacarbil in Japanese Restless Legs Syndrome Patients

Start date: December 2007
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of ASP8825 (gabapentin enacarbil) for long-term treatment of restless legs syndrome patients.

NCT ID: NCT02658175 Completed - Clinical trials for Familial Chylomicronemia Syndrome

The Approach Open Label Study: A Study of Volanesorsen (Formerly IONIS-APOCIIIRx) in Participants With Familial Chylomicronemia Syndrome

Start date: December 23, 2015
Phase: Phase 3
Study type: Interventional

An open-label study of volanesorsen (ISIS 304801) administered subcutaneously to participants with FCS.

NCT ID: NCT02657629 Completed - Clinical trials for Hypoplastic Left Heart Syndrome

Comparison of Feeding Strategies for Hypoplastic Left Heart Syndrome Infants

Start date: December 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if a continuous feeding regimen as compared to an intermittent bolus feeding regimen leads to improved weight gain in infants with hypoplastic left heart syndrome (HLHS) after stage 1 procedures.

NCT ID: NCT02655718 Recruiting - Clinical trials for Acute Coronary Syndrome

Short and Long Term Outcomes of Acute Coronary Syndrome in Patients With Non Obstructive Coronary Atherosclerosis

NOCA
Start date: October 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to assess short and long term outcomes of acute coronary syndrome in patients with non obstructive coronary atherosclerosis, to optimize the algorithm for diagnosis and to evaluate its effectiveness

NCT ID: NCT02654548 Completed - Clinical trials for Polycystic Ovary Syndrome

Sebum Excretion in Neonates of Women With Polycystic Ovary Syndrome (PCOS)

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

To investigate whether women with polycystic ovary syndrome who are post-partum excrete higher levels of sebum in comparison to healthy controls due to high levels of androgens.

NCT ID: NCT02653911 Not yet recruiting - Clinical trials for Polycystic Ovary Syndrome

Electroacupuncture on Menstrual Frequency in Women With Polycystic Ovary Syndrome: Study Protocol

Start date: January 2021
Phase: N/A
Study type: Interventional

Polycystic ovary syndrome (PCOS) is a dysfunction of endocrine system of women of reproductive age. Approximately 5%-10% women in China have this syndrome. Irregular menstruation (oligomenorrhea or amenorrhea), hirsutism and obesity are the common clinical manifestations of PCOS. The aim of this study is to evaluate the efficacy of acupuncture in improving the menstrual frequency of PCOS patients who do not have fertility requirements.

NCT ID: NCT02653495 Terminated - Metabolic Syndrome Clinical Trials

Impact of Metabolic Syndrome on Flu Vaccine Efficacy

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

Metabolic syndrome (MetS) is a cluster of metabolic conditions associated with obesity that predispose individuals to coronary heart diseases and diabetes but obesity has been shown to increase the risks of other diseases like cancer and asthma. Studies have also shown that obesity increases the risk of severe influenza infection and associated death and reduces the efficacy of influenza vaccine in the obese population but yet, the molecular mechanisms have not been described. The investigators are thus hypothesizing that differences in the innate immune responses between individual with or without metabolic syndrome impact viral infection and vaccine outcome. The investigators will perform seasonal influenza vaccination in people with or without metabolic syndrome to determine if the late adaptive response assessed by antibodies titers is different between the two groups and correlates with the early immune response assessed by gene expression profile in whole blood cells. The project proposed by the investigators will contribute to a better understanding of the inflammatory phenotype associated with metabolic syndrome and establish for the first time if it affects the immune protection against infectious diseases and particularly against influenza virus infection. The results will be important to determine if the population affected by metabolic syndrome should receive anti-influenza treatment in priority in the context of a severe influenza epidemic.

NCT ID: NCT02653131 Terminated - Clinical trials for Short Bowel Syndrome

The Use of DPP-4 Inhibitors in Short Bowel Syndrome

DPP-4
Start date: January 2016
Phase: Phase 4
Study type: Interventional

The inhibition of Dipeptidyl peptidase-4 should increase the concentration of glucagone-like peptide 1 and 2, and the increase of the latter should increase the absorptive capacity of the intestine.

NCT ID: NCT02652390 Completed - Clinical trials for Carpal Tunnel Syndrome

Local Steroid Injection vs Placebo in Carpal Tunnel Syndrome

Start date: February 2016
Phase: Phase 4
Study type: Interventional

Between 2008 and 2012 the investigators performed a single-center randomized double-blind placebo-controlled trial to assess the efficacy of local injection of two different doses of methylprednisolone (80 mg and 40 mg) in patients with carpal tunnel syndrome (CTS), aged 18 to 70 years, not previously treated with steroid injection. The primary outcomes were change in the CTS symptom severity score at 10 weeks and rate of carpal tunnel release surgery on the study hand at 1 year. In the trial 111 patients were randomized (37 in each of the 3 groups: 80 mg methylprednisolone, 40 mg methylprednisolone and placebo) and all completed the 1-year follow-up. The investiators plan an extended follow-up 5 to 7 years after injection.