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Connective Tissue Diseases clinical trials

View clinical trials related to Connective Tissue Diseases.

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NCT ID: NCT02392130 Completed - Clinical trials for Connective Tissue Diseases

A Clinical Trial to Assess the Potential of LEO 130852A Gel to Reduce Steroid Induced Skin Atrophy on Healthy Skin

Start date: March 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the effect of LEO 130852A gel 1% in maintaining skin thickness in healthy skin treated with steroid.

NCT ID: NCT02379793 Completed - Clinical trials for Skin and Connective Tissue Diseases

Skin Irritation Test of LEO 80185 Gel in Healthy Japanese Subjects

Start date: March 2015
Phase: Phase 1
Study type: Interventional

The purpose of the study is to investigate skin irritation of LEO 80185 gel, gel vehicle and Liquid Paraffin in healthy Japanese male subjects.

NCT ID: NCT02355639 Completed - Clinical trials for Skin and Connective Tissue Diseases

A Single-Centre Clinical Trial to Assess Steroid Induced Skin Atrophy on Healthy Skin

Start date: January 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess steroid induced skin atrophy by sonography.

NCT ID: NCT02298777 Recruiting - Vascular Disease Clinical Trials

Metabolomic Analysis of Systemic Sclerosis

SCLEROMICS
Start date: December 2014
Phase:
Study type: Observational

Currently investigators do not have diagnostic and prognostic markers for SSc which almost always starts with a vascular disease (Raynaud's disease) isolated for several years. The primary purpose is to highlight discriminating metabolic profiles depending on the characteristics of the disease, allowing early diagnosis of SSc at the onset of vascular lesions, by comparing the profiles of SSc beginners (<3 years) to established forms (> 3 years). Secondary purposes: - Prognosis: to study the metabolomics profile of SSc when a visceral complication occurs - Diagnosis: to compare the metabolomics profile of SSc to undifferentiated connective tissue disease (UCDT), Raynaud's disease (RD), vascular disease (VD) and healthy controls - Exploratory: to compare the metabolomics profile of blood, urine and skin of SSc patients

NCT ID: NCT02255695 Completed - Clinical trials for Musculoskeletal and Connective Tissue Disorders

Effects of a School-based Exercise Program on Posture, Trunk Range of Motion, and Musculoskeletal Pain

Start date: December 2008
Phase: N/A
Study type: Interventional

The objective of this study was to evaluate the effects of a school-based exercise program on posture, trunk range of motion and musculoskeletal pain in schoolchildren. This study was a Randomized controlled trial. The hypothesis was that the exercise group would have the postural deviations corrected, would have the trunk range of motion increased and would have the prevalence of pain decreased, while the control group would have not. Three schools from Brazil participated. The students that have been included (n=300) were randomly allocated to experimental (EG) or control group (CG). The intervention for EG consisted in a program based on stretching and strengthening exercises, applied twice a week, for eight weeks, with group sessions of 50 minutes. CG did not perform any intervention. Qualitative and quantitative postural evaluation (PAS/SAPO), musculoskeletal pain (self-report) and trunk mobility were collected.

NCT ID: NCT02234388 Recruiting - Clinical trials for Undifferentiated Connective Tissue Disease

Undifferentiated Connective Tissue Disease Registry

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

This registry has been established to gain a better understanding of the clinical and emotional presentations of patients with undifferentiated connective tissue disease.

NCT ID: NCT02198651 Completed - Clinical trials for Rheumatoid Arthritis

A Phase 4 Trial Assessing the ImPact of Residual Inflammation Detected Via Imaging TEchniques, Drug Levels and Patient Characteristics on the Outcome of Dose TaperIng of Adalimumab in Clinical Remission Rheumatoid ArThritis (RA) Subjects

PREDICTRA
Start date: January 5, 2015
Phase: Phase 4
Study type: Interventional

The primary objective of the study was to investigate the association between residual disease activity at Baseline as detected by Magnetic Resonance Imaging (MRI) and the occurrence of flares in participants with rheumatoid arthritis (RA) randomized to an adalimumab dose tapering regimen controlled by adalimumab withdrawal.

NCT ID: NCT01889966 Completed - Clinical trials for Pulmonary Hypertension Associated With Connective Tissue Disease

VasoREACTivity Testing With Intravenous SILdenafil in Patients With Precapillary Pulmonary Hypertension

SIL-REACT
Start date: April 2013
Phase: Phase 4
Study type: Interventional

Sildenafil is a selective pulmonary vasodilator; in patients with a special kind of pulmonary hypertension it is approved for treatment. The trial seeks to find out, whether the acute response to this treatment (= vasoreactivity testing) given intravenously is effective and allows prediction of therapy success during a following oral treatment.

NCT ID: NCT01862926 Completed - Clinical trials for Interstitial Lung Disease

Rituximab Versus Cyclophosphamide in Connective Tissue Disease-ILD

RECITAL
Start date: November 2014
Phase: Phase 2/Phase 3
Study type: Interventional

Interstitial lung disease (ILD) is characterised by inflammation and scarring of the lung and is the leading cause of death in patients with systemic sclerosis, and contributes significantly to morbidity and mortality in many other connective tissue diseases (CTDs) such as polymyositis/dermatomyositis and mixed connective tissue disease. When ILD is extensive and/or progressive, immunosuppressive medication is often required to stabilize lung disease and alleviate symptoms. Current standard care for CTD associated ILD is extrapolated from studies performed in individuals with systemic sclerosis and comprises low dose corticosteroids and intravenous cyclophosphamide followed by oral azathioprine. In some individuals even this intensive immunosuppression is insufficient to prevent deterioration, and in a significant minority of affected individuals this results in respiratory failure and death. Rituximab has recently been reported as an effective 'rescue therapy' for stabilizing and even improving ILD in this patient group. Based on observations gained from this experience, the investigators believe that rituximab is a potential important alternative to current best therapy for this patient group. This study has therefore been initiated to evaluate the efficacy of rituximab (compared with standard therapy) in patients with progressive CTD related ILD.

NCT ID: NCT01852851 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

Employment and Arthritis: Making it Work

MIW
Start date: June 2013
Phase: N/A
Study type: Interventional

The investigators plan to conduct a randomized controlled trial to evaluate the effectiveness and the cost effectiveness of an on-line eLearning program (entitled Employment and Arthritis: Making it Work) designed to help people with inflammatory arthritis stay employed. The program also includes assessments with 1) an occupational therapist, and 2) a vocational rehabilitation counsellor at the end of the program to help participants identify and obtain necessary changes at work. People from three provinces will be recruited from collaborators' patient and program recipient lists. The study group will receive the program intervention and the control group will receive "usual care" and printed educational material. All participants will be followed for five years. The effectiveness of the program at improving at work productivity and reducing work cessation will be evaluated compared to a control group receiving printed material on employment and arthritis.