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Syndrome clinical trials

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NCT ID: NCT02408094 Recruiting - Clinical trials for Arthritis, Rheumatoid

Screening Protein Markers in Patients With Rheumatoid Arthritis and Hot-dampness and Blood Stasis Syndrome

Start date: May 2015
Phase: N/A
Study type: Observational

The purpose of this study is to explore the protein markers and to applicate those protein markers in syndrome diagnosis of hot-dampness and blood stasis syndrome in patients with RA.

NCT ID: NCT02407522 Completed - Clinical trials for Metabolic Syndrome X

The Improvements of Dietary Supplement of Black Rice on Metabolic Syndrome

IDSBRMS
Start date: June 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to thoroughly investigate how the interaction between black rice and human gut microbiota affects metabolic diseases, this study will recruit patients with Metabolic Syndrome (MS) and provide them with dietary supplementation of black rice (50 g/day) for 3 months to observe its effect on the development of MS. The focuses of this project are to elucidate how black rice consumption affects the composition and metabolism of intestinal bacteria as well as the development of MS, and to further analyze whether the changes in intestinal bacteria are associated with the changes in MS improvements.

NCT ID: NCT02403258 Recruiting - Tourette Syndrome Clinical Trials

The Effect and Safety of Plum-blossom Needle for Tourette Syndrome

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

To evaluate the effect and safety of plum-blossom needle for Tourette syndrome.

NCT ID: NCT02402530 Completed - Clinical trials for Complex Regional Pain Syndrome, Type I

Efficacy and Safety of Intravenous Neridronic Acid in CRPS-I

Start date: April 2015
Phase: Phase 2/Phase 3
Study type: Interventional

This clinical trial is being conducted to demonstrate the efficacy of neridronic acid in the treatment of pain associated with complex regional pain syndrome type I (CRPS-I). The trial is divided into 3 periods: a 60-day enrollment period, a 12-week trial period, and an extended follow-up period with visits at Month 6, Month 9, and Month 12. The extended follow-up period will be terminated for all participants after the last participant enrolled completes their Month 6 visit (Visit 9). The double-blind will be maintained throughout the 12-week trial period and extended follow-up period.

NCT ID: NCT02402400 Recruiting - Clinical trials for Acute Coronary Syndromes

Sub Lingual Versus Traditional Oral Administration of Ticagrelor in Acute Coronary Syndrome/Non ST-elevation Myocardial Infarction - A Platelet Reactivity Study

Start date: July 2015
Phase: Phase 4
Study type: Interventional

Our goal is to examine sub lingual versus traditional oral administration of ticagrelor in ACS/non ST-elevation Myocardial Infarction (NSTEMI) patients on platelet reactivity.

NCT ID: NCT02402309 Completed - Clinical trials for Sjögren-Larsson Syndrome

A Study of Topical NS2 Cream to Treat Ichthyosis in Sjögren-Larsson Syndrome (SLS)

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

This is a multi-center, randomized, double-blind, vehicle-controlled, parallel-group study designed to evaluate the safety, pharmacokinetic (PK), and exploratory activity of topically-applied NS2 dermatologic cream administered once-daily (QD) to subjects with ichthyosis secondary to Sjögren- Larsson Syndrome (SLS). NS2 is expected to trap fatty aldehydes that are pathogenic in SLS patients, and thereby diminish the lipid-aldehyde adduct formation that likely results in ichthyosis associated with SLS, and potentially reduce the mild dermal inflammation characteristic of SLS.

NCT ID: NCT02402049 Not yet recruiting - Clinical trials for Premenstrual Syndrome-PMS

Homeopathic Treatment of Premenstrual Syndrome

Start date: March 2015
Phase: Phase 3
Study type: Interventional

The proposed study will focus on premenstrual syndrome (PMS) symptom alleviation for women diagnosed as suffering from the syndrome with the DRSP questionnaire. The women will be treated with Homeopatic remedies. The improvement of PMS symptoms will be evaluated using the Daily Record of Severity of Problems questionnaire (DRSP). The questionnaire will be completed daily by women for 2 months prior to receiving the treatment and for 3 months following treatment with a single dose of the homeopathy treatment.

NCT ID: NCT02400463 Completed - Clinical trials for Hemophagocytic Syndrome (HPS)

A Pilot Study of Ruxolitinib in Secondary Hemophagocytic Syndrome

Start date: February 5, 2016
Phase: Phase 2
Study type: Interventional

This is a pilot study to determine the efficacy of Ruxolitinib in secondary hemophagocytic syndrome. The primary objective is to assess the efficacy of ruxolitinib 15 mg PO twice daily in patients with HPS. The primary endpoint is overall survival at two months.

NCT ID: NCT02399527 Recruiting - Clinical trials for Lymphatic Malformation

Lymphatic Anomalies Registry for the Assessment of Outcome Data

Start date: June 2013
Phase:
Study type: Observational [Patient Registry]

Lymphatic anomalies are a rare subset of vascular anomalies that are poorly understood. the understanding of the natural history, long-term outcomes, risk factors for morbidity and mortality, and the relative benefit of medical therapies and procedures is limited.The goal of this project is to better understand these diseases and improve the care of theses rare patients. To do this, the investigators are conducting an observational study of patients with lymphatic anomalies, including an annual follow-up questionnaire to gather prospective data on mortality, morbidity, treatments, and functionality as well as quality of life.

NCT ID: NCT02398604 Terminated - Clinical trials for Hypoplastic Left Heart Syndrome

Allogeneic hMSC Injection in Patients With Hypoplastic Left Heart Syndrome

ELPIS
Start date: April 2015
Phase: Phase 1
Study type: Interventional

This study is intended to evaluate the safety and feasibility of intramyocardial injection of allogeneic mesenchymal cells during the Bi-Directional Cavopulmonary Anastomosis (BDCPA) surgery for hypoplastic left heart syndrome (HLHS) pediatric patients.