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Syndrome clinical trials

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NCT ID: NCT02335268 Completed - Clinical trials for Myelodysplastic Syndromes

Validation of a Predictive Model of Response to Romiplostim in Patients With IPSS Low or Intermediate-1 Risk MDS and Thrombocytopenia

EUROPE
Start date: May 21, 2015
Phase: Phase 2
Study type: Interventional

There are currently no licensed drugs in the EU to treat thrombocytopenia in MDS patients classified as IPSS low/int-1. Prior studies with romiplostim (a TPO receptor agonist) in MDS found that baseline concentration of TPO as well as transfusion history were predictive of subsequent response in a retrospective model. The current prospective study has the aim to explore whether both pretreatment variables (endogenous TPO, TPO-level, platelet transfusion history) can predict the response to subsequent short-term treatment with romiplostim.

NCT ID: NCT02335216 Terminated - Clinical trials for Failed Back Surgery Syndrome

A Post Market Study on Dorsal Root Ganglion (DRG) Stimulation in Failed Back Surgery Syndrome (FBSS)

SYMPATHY
Start date: January 2014
Phase:
Study type: Observational

18-SMI-2013 is a post market, observational, questionnaire based study to assess the effectiveness of the commercially available Axium neurostimulator in the management of chronic pain following lumbar discectomy (Failed Back Surgery Syndrome)

NCT ID: NCT02334306 Completed - Clinical trials for Primary Sjögren's Syndrome

A Phase 2a, Randomized, Placebo Controlled, Study to Evaluate the Safety and Efficacy of AMG 557/MEDI5872 in Primary Sjögren's Syndrome

Start date: June 8, 2015
Phase: Phase 2
Study type: Interventional

A Phase 2a study to evaluate the efficacy and safety of AMG 557/MEDI5872 in Primary Sjögren's Syndrome

NCT ID: NCT02333760 Active, not recruiting - Clinical trials for Wiskott-Aldrich Syndrome

Long Term Safety Follow up of Haematopoietic Stem Cell Gene Therapy for the Wiskott Aldrich Syndrome

WASFUP
Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

An open follow up study of patients enrolled in the Phase 1/2 clinical trial of haematopoietic stem cell gene therapy for the Wiskott-Aldrich Syndrome and treated with autologous CD34+ cells transduced with the w1.6_hWASP_WPRE (VSVg) lentiviral vector.

NCT ID: NCT02333669 Completed - Clinical trials for Neonatal Respiratory Distress Syndrome

Association of SCNN1A Single Nucleotide Polymorphisms With Neonatal Respiratory Distress Syndrome

Start date: January 2012
Phase: N/A
Study type: Observational

Lung fluid absorption disorders are largely mediated by transepithelial Na+ reabsorption through alpha epithelial sodium channels (α-ENaCs) in alveolar epithelial cells. Increasing evidence has demonstrated that these lung disorders might be an important cause of neonatal respiratory distress syndrome (NRDS) by influencing gas exchange or surfactant function, particularly in near-term and term infants. The SCNN1A gene, which encodes the α-ENaC, might predispose infants to NRDS. To explore whether the single-nucleotide polymorphisms (SNPs) of SCNN1A are associated with NRDS, we conducted a case-control study to investigate the NRDS-associated loci in Han Chinese infants. Seven target SNPs were selected from the SCNN1A gene and were genotyped using the improved multiplex ligase detection reaction (iMLDR).

NCT ID: NCT02333617 Terminated - Clinical trials for Patellofemoral Pain Syndrome

Manual Therapy to Treat Gluteus Medius Trigger Points

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

This is a blinded randomized controlled trial to assess the effectiveness of manual therapy to improve hip abduction strength in patients with acute anterior knee pain. The primary objective of this study is to see if manual therapy to the gluteus medius can significantly alter within-session measurements of hip abductor strength in patients with anterior knee pain. The secondary objective of this study is to see if manual therapy to the gluteus medius can significantly alter within session pain in patients with anterior knee pain.

NCT ID: NCT02332655 Completed - Clinical trials for Sturge-Weber Syndrome

Cannabidiol Expanded Access Study in Medically Refractory Sturge-Weber Syndrome

Start date: December 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the tolerability and optimal dose of cannabidiol (CBD) as an simultaneous treatment in children and young adults with Sturge-Weber syndrome (SWS) and drug resistant epilepsy.

NCT ID: NCT02330692 Recruiting - Clinical trials for Myelodysplastic Syndrome

Cohort Study of New Prognostic Factors With Peripheral Blood and Bone Marrow Evaluation at the Time of Diagnosis and Relapse in Myelodysplastic Syndrome

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

Developing a molecular genetic test that can identify prognostic factors which can predict response to treatment, and to contribute to the establishment of future therapeutic strategies base on prognostic factors by undergoing peripheral blood and bone marrow examination of Myelodysplastic Syndrome (MDS) patients at diagnosis and relapse.

NCT ID: NCT02330328 Withdrawn - Clinical trials for Acute Coronary Syndrome

Telemetry for Chest Pain of Low Risk for Acute Coronary Syndrome Pts

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

This is a randomized controlled, multi-center, non-blinded non-inferiority study examining the utility of telemetry monitoring in patients admitted who are low risk for acute coronary syndrome. Each of the six sites will prospectively enroll 250 patients in each arm of the study randomized to either a med-surg bed (no telemetry) or a telemetry bed during their admission. Research study coordinators will enroll patients and then follow them throughout their hospital course and record primary and secondary end point events.

NCT ID: NCT02330029 Active, not recruiting - Clinical trials for Irritable Bowel Syndrome

Pinaverium and Herbs for Irritable Bowel Syndrome Treatment: an Onset and Offset Study (PHIBEST)

Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to test the onset of action, offset of action, efficacy, and safety of pinaverium and an herbal medication for irritable bowel syndrome (IBS) for a long term (over one year). Pinaverium has been in many countries, but there is no randomized, double-blind, large sample size, and placebo-controlled study on this medication yet. Tong Xie Yao Fang (Formula for pain and diarrhea) is a historically and contemporarily used traditional Chinese medicine that can be used for IBS. The hypothesis is that the two remedies are effective and safe for IBS treatment with no significant different onset and offset of actions when tested by modern clinical standards and criteria.