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Syndrome clinical trials

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NCT ID: NCT02309632 Withdrawn - Clinical trials for Pancreatic Neoplasms

Pancreatic Cancer Screening of High-Risk Individuals in Arkansas

Start date: November 2015
Phase: N/A
Study type: Interventional

100 subjects who have a family history of pancreatic cancer (PC), or known genetic syndromes associated with increased risk of pancreatic cancer, will be followed for five years. This data will be used to determine the pancreatic cancer and precancerous lesion detection rate in High Risk Individuals (HRIs). Subjects may agree to annual imaging and annual biomarkers or to biomarkers only.

NCT ID: NCT02308761 Completed - Clinical trials for Acute Myeloid Leukemia

A Study of RO6870810/TEN-010 in Participants With Acute Myeloid Leukemia and Myelodysplastic Syndrome

Start date: November 6, 2014
Phase: Phase 1
Study type: Interventional

RO6870810 (formerly TEN-010) is a small molecule, bromodomain and extra-terminal (BET) bromodomain inhibitor. This study is designed to characterize the safety, tolerability, and pharmacokinetics of RO6870810 monotherapy in participants with relapsed/refractory acute myeloid leukemia (RR-AML) and hypomethylating agent (HMA)-refractory myelodysplastic syndrome (MDS). The study will consist of a Screening Period, Treatment Period, and Post-Treatment Period. A standard 3+3 design will be used in which successive cohorts of three or more participants with RR-AML or HMA-refractory MDS will be treated at escalating doses until a maximum tolerated dose (MTD) is identified. Up to 51 adult participants with AML or MDS will be enrolled in the study.

NCT ID: NCT02307214 Completed - Clinical trials for Takotsubo Cardiomyopathy

Tako-Tsubo Cardiomyopathy and Cardiac Syndrome X: New Insights Into the Pathophysiology

ENDAUT
Start date: October 2013
Phase: N/A
Study type: Interventional

Tako-Tsubo Cardiomyopathy (TTC) and Cardiac Syndrome X (CSX) are respectively acute and chronic cardiac conditions whose clinical presentation, mimicking the onset of acute myocardial ischemia in absence of epicardial coronary disease, has progressively gained the interest of the scientific community. However, despite significant progress, their underlying pathophysiology, which seems to evoke some similarities, still remains elusive. Endothelial dysfunction and autonomic imbalance have both been individually implied in their puzzling pathogenesis. The investigators plan to conduct our study in a cohort of TTC patients, CSX patients and healthy volunteers with the following primary objective: to assess the response of endothelial function (through the Endopat score) to the autonomic tone activation induced by a 10-minute stress mental test. The assessment of autonomic tone during activation through the evaluation of Spontaneous BaRoreflex Sensitivity (BRS) and its correlation with endothelial function (Endopat score) will represent secondary objectives. Our study will enroll 15 patients with TTC at least six months after the event, 15 patients with classic CSX and 15 healthy volunteers who will serve as control.

NCT ID: NCT02306616 Completed - Clinical trials for Acute Coronary Syndrome

CCC Project- Acute Coronary Syndrome

Start date: November 2014
Phase:
Study type: Observational

To develop and implement quality improvement programs for the treatment of acute coronary syndrome (ACS) in China based on the successful experience of the AHA-Get with the Guidelines program. This program will use data collection, analysis, feedback, and process improvement to extend the use of evidence-based guidelines throughout the healthcare system and improve patient care of acute coronary syndrome.

NCT ID: NCT02306369 Completed - Clinical trials for Irritable Bowel Syndrome

Internet-delivered CBT for Irritable Bowel Syndrome in Adolescents

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

This randomized controlled trial aims to evaluate the treatment effects of an internet-delivered CBT-program for adolescents with irritable bowel syndrome.

NCT ID: NCT02305680 Completed - Clinical trials for Acute Coronary Syndromes

Long-term Follow-up of antithrombotIc Management Patterns in Acute Coronary Syndrome Patients in Asia-China Extension

EPICOR
Start date: December 17, 2014
Phase:
Study type: Observational

This study is to describe the long-term antithrombotic management patterns in a real-life setting for patients hospitalized with an acute coronary syndrome in China.

NCT ID: NCT02304367 Completed - Clinical trials for Tumor Induced Osteomalacia (TIO)

Study of Burosumab (KRN23) in Adults With Tumor-Induced Osteomalacia (TIO) or Epidermal Nevus Syndrome (ENS)

Start date: March 24, 2015
Phase: Phase 2
Study type: Interventional

The primary objectives of this study are to evaluate the effect of burosumab treatment on: - Increasing serum phosphorus levels in adults with TIO or ENS-associated osteomalacia - Improvement in TIO/ENS-associated osteomalacia as determined by osteoid thickness (O.Th), osteoid surface/bone surface (OS/BS), osteoid volume/bone volume (OV/BV) and mineralization lag time (MLt).

NCT ID: NCT02304302 Completed - Down Syndrome Clinical Trials

Down Syndrome Memantine Follow-up Study

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

The purpose of this research study is to learn if the medication Memantine Hydrochloride (the study medication) can help adolescents and young adults with Down syndrome. Dr. Alberto Costa and his research team want to see if a 16-week treatment with this medication can improve the participant's ability to learn and remember things. In this study, memantine hydrochloride will be used. Thus, the researchers want to learn whether the study drug can help improve memory in young adults with Down syndrome. To test the effect of the study medicine, half of the people in the study will receive the study medicine and half will receive a placebo (an inactive substance). Memantine is an approved medication to treat memory and thinking problems in persons with Alzheimer disease. However, little is known about the effect of this medication in persons with Down syndrome and it has not been approved for use in persons with Down syndrome.

NCT ID: NCT02303470 Active, not recruiting - Insulin Resistance Clinical Trials

PCOS & Insulin Resistance Exercise Study

Start date: March 2015
Phase: N/A
Study type: Interventional

This study evaluates the feasibility and metabolic effects of implementing a structured exercise program in women with polycystic ovary syndrome and insulin resistance. Participants will be randomized to either 75 minutes of vigorous exercise or 150 minutes of moderate exercise per week.

NCT ID: NCT02303171 Recruiting - Clinical trials for Antiphospholipid Syndrome

Use of Warfarin After the First Trimester in Pregnant Women With APS

Start date: November 2014
Phase: Phase 4
Study type: Interventional

Evaluation of shifting to oral vitamin K antagonist after the first trimester instead of using low molecular weight heparin (LMWH) throughout pregnancy in pregnant women with antiphospholipid syndrome (APS)