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NCT ID: NCT01584713 Recruiting - Clinical trials for Enterocutaneous Fistula

Stromal Vascular Fraction (SVF) for Treatment of Enterocutaneous Fistula (HULPUTC)

HULPUTC
Start date: December 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine safety of Stromal Vascular Fraction (SVF) for the treatment of enterocutaneous fistula.

NCT ID: NCT01574053 Recruiting - Clinical trials for Huntington's Disease

Enroll -HD: A Prospective Registry Study in a Global Huntington's Disease Cohort

Start date: July 2012
Phase:
Study type: Observational [Patient Registry]

Enroll-HD is a longitudinal, observational, multinational study that integrates two former Huntington's disease (HD) registries-REGISTRY in Europe, and COHORT in North America and Australasia-while also expanding to include sites in Latin America. More than 30,000 participants have now enrolled into the study. With annual assessments and no end date, Enroll-HD has built a large and rich database of longitudinal clinical data and biospecimens that form the basis for studies developing tools and biomarkers for progression and prognosis, identifying clinically-relevant phenotypic characteristics, and establishing clearly defined endpoints for interventional studies. Periodic cuts of the database are now available to any interested researcher to use in their research - visit www.enroll-hd.org/for-researchers/access-data/ to learn more.

NCT ID: NCT01554722 Recruiting - Clinical trials for Peripheral Nerve Injury

Needle Nerve Contact in Ultrasound Guided Femoral Block

Start date: November 2011
Phase: N/A
Study type: Interventional

Ultrasound-guided femoral nerve block is a common regional anesthesia technique. The optimal method of needle guidance (in-plane versus out-of-plane) with regards to the block efficacy and avoidance of needle-nerve contact has not been established. In this study the investigators tests the hypothesis that the incidence of needle-nerve contact is higher with the needle insertion in an out-of-plane than with the in-plane approach.

NCT ID: NCT01550575 Recruiting - Chronic Pain Clinical Trials

Patient Retrospective Outcomes (PRO)

PRO
Start date: April 3, 2012
Phase:
Study type: Observational

This study will evaluate de-identified (anonymous) data in subject medical charts to review the clinical outcomes of various treatment approaches in the treatment of chronic pain.

NCT ID: NCT01548092 Recruiting - Clinical trials for Recto-vaginal Fistula

Stromal Vascular Fraction (SVF) for Treatment of Recto-vaginal Fistula

HULPCIR
Start date: December 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine safety of Stromal Vascular Fraction (SVF) for the treatment of recto-vaginal fistula.

NCT ID: NCT01542580 Recruiting - Clinical trials for Rheumatoid Arthritis

A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee

Start date: March 2012
Phase:
Study type: Observational

The purpose of this study is to evaluate performance of the Vanguard 360 revision knee system utilizing offset on either the tibial component, femoral component, or both in terms of the restoration of mechanical alignment, clinical outcomes and survivorship.

NCT ID: NCT01538082 Recruiting - Metabolic Syndrome Clinical Trials

Role of the Stress in the Development of the Metabolic Syndrome

STREX
Start date: December 2008
Phase: N/A
Study type: Observational

The purpose of this study is determine the incidence of metabolic syndrome (MetS) in people of high risk, of 40 or more years and attended in the Primary Care. Evaluating the association between anxiety, depression, quality of life and the vital stressful events, and the development of the metabolic syndrome in general population. Our hypothesis is that population of the cohort with bigger degree of stress will develop earlier the metabolic syndrome. If our hypothesis about the metabolic syndrome are demonstrated, it would allow establishing in a future interventions on these factors of risk to prevent or to decrease the incidence of this syndrome in the Primary Care.

NCT ID: NCT01537016 Recruiting - Clinical trials for Diabetic Foot Ulcers

WOUNDCHEK™ Protease Status Point of Care (POC) Diagnostic Test on DFU

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

The purpose of this trial is to determine if wounds with elevated protease activity (EPA) treated with targeted interventions such as protease modulating therapies can improve clinical and economic outcomes. It is hypothesized that protease modulating dressings may provide significantly better clinical outcomes on EPA wounds over current standard of care.

NCT ID: NCT01524276 Recruiting - Clinical trials for Coronary Artery Disease

Product Surveillance Registry

PSR
Start date: January 2012
Phase:
Study type: Observational

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.

NCT ID: NCT01522183 Recruiting - Clinical trials for Atypical Hemolytic-Uremic Syndrome

Atypical Hemolytic-Uremic Syndrome (aHUS) Registry

Start date: April 30, 2012
Phase:
Study type: Observational [Patient Registry]

Post-marketing safety data on patients treated and untreated with eculizumab or ravulizumab.