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Syndrome clinical trials

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NCT ID: NCT02983123 Completed - Clinical trials for Acute Coronary Syndrome

One-hour Troponin in a Low-prevalence Population of Acute Coronary Syndrome

OUT-ACS
Start date: November 15, 2016
Phase:
Study type: Observational

This study aims to evaluate if the 1-hour rule-in/rule-out algorithm for a high-sensitivity cardiac troponin T (hs-cTnT) is safe and effective for use in the primary care where the patients have a lower pretest probability of an acute myocardial infarction (MI). During this study troponins will be collected at 0-, 1- and 4/6-hours, where absolute changes in the values will decide whether the patient need hospitalization or not.

NCT ID: NCT02980913 Completed - Dry Eye Syndromes Clinical Trials

Difference in the Frequency of Use of Lachrymal Substitutes in Patients With Moderate to Severe Dry Eye Syndrome

Start date: February 11, 2016
Phase: N/A
Study type: Interventional

Dry eye syndrome is a highly prevalent ocular disease with an increasing incidence in the elderly population. Topically administered lubricants are the basis for treatment of this disease. Relief of symptoms in patients with moderate to severe dry eye disease is usually reached by the use of artificial tears during the day. Nighttime relief is often achieved by substances known to be more adhesive to the ocular surface, such as gels.

NCT ID: NCT02980770 Recruiting - Clinical trials for Obstructive Sleep Apnea

Postoperative Complications in Patients With Obesity Hypoventilation Syndrome

OHBE
Start date: November 2016
Phase: N/A
Study type: Observational

Obstructive sleep apnea (OSA) and Obesity-Hypoventilation Syndrome (OHS) are common conditions in obesity, which may influence the prognosis in patients undergoing surgery. There is a need for simple screening tools to identify such patients at high risk. The current multicenter observational study aims to investigate occurrence of OSA and OHS in obese individuals undergoing elective abdominal surgery and further address its impact on perioperative and postoperative complications.

NCT ID: NCT02980666 Completed - Clinical trials for Short Bowel Syndrome

Study in Japanese Pediatric Subjects With Short Bowel Syndrome (SBS) Who Are Dependent on Parenteral Support

Start date: January 13, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if an investigational treatment (teduglutide) is safe and effective in Japanese children (age 4 months through 15 years of age) with SBS who are dependent on parenteral support. This study will also evaluate how teduglutide moves through the body (pharmacokinetics) and how it affects the body (pharmacodynamics).

NCT ID: NCT02979366 Completed - Clinical trials for Myelodysplastic Syndrome (MDS)

Phase I Study of S64315 Administred Intravenously in Patients With Acute Myeloid Leukaemia or Myelodysplastic Syndrome

Start date: March 15, 2017
Phase: Phase 1
Study type: Interventional

The CL1-64315-001 study is a phase I, international, multicentre, open-label, non-randomised, non-comparative study. This study is designed in two parts: one part for dose escalation, one part for dose expansion.

NCT ID: NCT02978079 Recruiting - Stroke Clinical Trials

Pupillometry in Horner's Syndrome

Start date: February 15, 2017
Phase: N/A
Study type: Interventional

Horner's syndrome (HS) is a result of interruption of the sympathetic innervation to the eye and ocular adnexa, which can occur due to carotid artery dissection (CAD), along which the sympathetic nerve fibers travel to reach the eye. Dissection of the carotid artery is one of the etiologies for ischemic stroke in young patients. In our current study, we will explore the diagnostic accuracy of automated binocular pupillometry in the diagnosis or HS, and its potential in identifying dissection of the carotid artery in patients of young age who suffer ischemic stroke.

NCT ID: NCT02977975 Completed - Clinical trials for Irritable Bowel Syndrome

Lacto-fermented Sauerkraut in the Treatment of Irritable Bowel Syndrome

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

The aim of the present study is to assess the efficacy of traditionally fermented sauerkraut in the treatment of irritable bowel syndrome.

NCT ID: NCT02977845 Completed - Clinical trials for Lung Cancer, Nonsmall Cell

Effect of Qigong on the Symptom Clusters of Dyspnea, Fatigue, and Anxiety.

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Effects of Qigong on symptom clusters of dyspnea, fatigue, and anxiety in Vietnamese lung cancer patients: A randomized control trial

NCT ID: NCT02975908 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome

A Realworld Study of Acute Respiratory Distress Syndrome in China

CHARDSnet
Start date: August 2015
Phase: N/A
Study type: Observational

ARDS is a critical respiratory disease caused by endogenous and exogenous factors. The mortality of ARDS varies from 30 to 70%. In 2012, a new international diagnostic criterion has been put forward. Yet, its feasibility, reliability and validity need to be tested. Meanwhile, the correlation of different severity and prognosis remains unclear. As so far, the epidemiological information about ARDS in China is lacking. Investigators plan to conduct a multi-center observational study(real-life study) to investigate the risk factors, morbidity, management and prognosis of ARDS in China, in order to facilitate standardization of diagnosis and management of ARDS and provide basic data and idea for further clinical intervention studies.

NCT ID: NCT02974907 Completed - Dry Eye Syndrome Clinical Trials

Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome : ARISE-2

Start date: November 2016
Phase: Phase 3
Study type: Interventional

The objective of this study is to compare the safety and efficacy of RGN-259 Ophthalmic Solutions to placebo for the treatment of the signs and symptoms of dry eye.