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Syndrome clinical trials

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NCT ID: NCT03296059 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome (ARDS)

Transfusion of Red Blood Cells for Acute Respiratory Distress Syndrome(ARDS) in Neonates

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

Acute respiratory distress syndrome (ARDS) in neonates has been defined in 2017. The death rate is over 50%.There are no special treatments for acute respiratory distress syndrome.

NCT ID: NCT03286634 Recruiting - Clinical trials for Acute Lymphoblastic Leukemia

ASIA Down Syndrome Acute Lymphoblastic Leukemia 2016

Start date: April 18, 2017
Phase: Phase 2
Study type: Interventional

To evaluate the outcome of a prednisolone and low dose methotrexate based protocol in Down syndrome children with ALL (DS-ALL) in an Asia-wide study. The treatment protocol was modified based upon backbone of Taiwan Pediatric Oncology Group (TPOG)-ALL protocol in which risk classification will be guided by level of flow minimal residual disease (MRD) instead.

NCT ID: NCT03286491 Recruiting - Clinical trials for Acute Coronary Syndrome

Clinical Decision Support System to Define 30 Day Adverse Clinical Events for Emergency Department Acute Coronary Syndromes

Start date: August 12, 2017
Phase: N/A
Study type: Observational

Acute coronary syndromes are among main complains for patients presenting to emergency department. Risk classification systems are used to classify patients to appropriate risks and help physicians manage diagnosis strategies and treatments. Purpose of this study is to develop a clinical decision support system for patients presenting to emergency department with the help of statistical machine learning.

NCT ID: NCT03281473 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Comparison of Positive End Expiratory Pressure Titration Methods in ARDS Patients

ELSE
Start date: October 2, 2018
Phase: N/A
Study type: Interventional

This study aims at assessing the short-term physiological effects of 2 positive end expiratory pressure titration strategies in patients with ARDS.

NCT ID: NCT03275480 Recruiting - Clinical trials for Myelodysplastic Syndromes

Institut Paoli Calmettes Myelodysplastic Syndromes Database

Start date: January 18, 2016
Phase:
Study type: Observational [Patient Registry]

Database of Institut Paoli-Calmettes patients diagnosed with Myelodysplastic Syndromes

NCT ID: NCT03268733 Recruiting - Clinical trials for Polycystic Ovary Syndrome

The Effects of Folic Acid on Sudanese Women With Polycystic Ovary Syndrome

FolicacidPCOS
Start date: September 1, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

An open clinical trial

NCT ID: NCT03262844 Recruiting - Clinical trials for Tethered Cord Syndrome

Efficacy and Safety of Nerve Root Axial Decompression Surgery in The Treatment of Tethered Cord Syndrome

Start date: June 16, 2017
Phase: N/A
Study type: Interventional

Background: Tethered cord syndrome (TCS) is a progressive clinical condition including a series of neurological dysfunctions and deformities attributable to abnormally increased tension on the spinal cord, which is lacking effective treatment to relieve the symptoms and prevent progression. Dr. Shi recently proposed a new technique as nerve root axial decompression surgery, which is also called capsule surgery, to treat patients with TCS. Yet, the effectiveness and safety should be further studied. Purpose: The aim of this study is to compare the effectiveness and safety of clinical outcomes between capsule surgery and conservative treatment in patients with TCS. A study hypothesis is that outcomes will be improved after capsule surgery. Methods: This study is a randomized clinical trial with a two-factor (2x7) research design. The TCS patients will be randomly assigned in one of the two treatment groups: capsule surgery and conservative treatment. Seven outcome measures will be collected pre-operative for baseline, and then at1, 12, 24, 48, and 96 weeks post-operative follow-up visits, including: International Consultation on Incontinence Modular Questionnaire Short Version (ICI-Q-SF), Rintala Score, a new developed Chinese version of questionnaire, Oswestry disability index (ODI), SF-12, foot function index (FFI) and Pirani score. Urodynamic testing, bladder ultrasonography, electromyogram, muscle strength and sensation of lower limbs will be obtained before and post treatment, to determine the patient`s function of lower limbs. The investigator performing the outcome measures will be blinded to group assignment, and therefore will not participate in treatment. After randomization, the conservative group will be followed up in the outpatient clinic. The capsule surgery group will receive the nerve root axial decompression surgery (capsule surgery). Data Analysis: Two 2x7 MANOVAs with repeated measures will be used to examine the differences in the seven measures between groups and at the five different time frames with the α level set at 0.05. Non-parametric tests (Mann-Whitney U tests) will be used to compare the differences in the urodynamics and muscle strength data over time and between groups.

NCT ID: NCT03259971 Recruiting - Tourette Syndrome Clinical Trials

The Role of Probiotics PS128 in Movement Disorders

Start date: August 25, 2017
Phase: N/A
Study type: Interventional

Pediatric movement disorders comprise of a large number of different neurological diseases including Rett syndrome (RTT) and Tourette syndrome. Studies in the literature as well as our preliminary reports showed that Rett syndrome and Tourette syndrome/Tic disorders are associated with a dysbiosis of the gut microbiota compared to normal control. Probiotic Lactobacillus plantarum PS128 is a diet supplement that available for human consumption. Probiotic Lactobacillus plantarum PS128 had showed psychotropic effects such as ameliorate anxiety- and depression-like behaviors as well as altered the level of neurotransmitters such as dopamine in the brain in animal models, which might be through microbiota-gut-brain axis. Therefore, the purpose of this study is to access the possible neurobehavior effects of Probiotic Lactobacillus plantarum PS128 in Rett syndrome and Tic disorders/Tourette syndrome.

NCT ID: NCT03251300 Recruiting - Clinical trials for Overactive Bladder Syndrome

Mirabegron for Female OAB Patients: Comparison of Daytime and Nighttime Dosing

Start date: August 1, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to elucidate whether night-time dosing of mirebegron can improve nocturia, compared with daytime dosing of mirabegron.

NCT ID: NCT03241394 Recruiting - Obesity Clinical Trials

The Monocyte Subsets in Obese Patients With and Without Metabolic Syndrome

Start date: July 25, 2017
Phase: N/A
Study type: Observational

Obesity is associated with a chronic low-grade inflammation characterized by macrophage infiltration in adipose tissue that induces insulin resistance and the appearance of metabolic syndrome (MS). The aim of the study was the investigation of whether circulating monocyte subsets are differentially regulated in MS.