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Sarcoidosis clinical trials

View clinical trials related to Sarcoidosis.

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NCT ID: NCT02459431 Completed - Sarcoidosis Clinical Trials

RCT Comparing 21 and 22 G Needle in the Diagnosis of Sarcoidosis by EBUS TBNA

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

Randomized controlled trial to determine the efficacy of different needles sizes (22G and 21G) used in endobronchial ultrasound guided transbronchial needle aspiration

NCT ID: NCT02405897 Completed - Sarcoidosis Clinical Trials

A Study to Evaluate the Efficacy and Safety of Fenestrated Cup Forceps Versus Fenestrated Alligator Forceps for Performing Transbronchial Lung Biopsy in Patients With Sarcoidosis

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

Sarcoidosis is a systemic disease that results from granulomatous inflammation that involves multiple body organs. The diagnosis requires the presence of compatible clinicoradiological features along with histologic evidence that demonstrates non-caseating.1 Mediastinal lymph nodes and the lung parenchyma are the most commonly involved structures in sarcoidosis that can be sampled by, performing various bronchoscopic techniques. In a recent study the use of alligator forceps had a better yield in comparison to cup forceps. The investigators hypothesize that use of fenestrated alligator forceps in comparison to fenestrated cup forceps will yield larger samples, thereby improving the diagnostic yield and reducing the number of biopsy samples irrespective of the stage of sarcoidosis.

NCT ID: NCT02361281 Enrolling by invitation - Sarcoidosis Clinical Trials

Validation of a Non-invasive Diagnostic Method for Sarcoidosis Using Exhaled Breath

Start date: December 2014
Phase: N/A
Study type: Observational

Sarcoidosis is a chronic lung disease that is characterized by fatigue, shortness of breath, chest pain and reduced lung function. Suffering from these diseases has a very negative effect on the quality of life. When people are suspected of having sarcoidosis various markers in the blood are measured. Ultimate diagnosis, however, always requires invasive techniques such as bronchoscopy and lung biopsy. Consequently, there is an urgent need for a new diagnostic tool that is easy, quick and most of all non-invasive and thus friendly for the patient. Such a new diagnostic tool might be found in examining the exhaled air of patients, which contains a complex mixture of so-called volatile organic compounds (VOCs) that are the result of damaging processes that occur in the lung. Determining the VOC profile in the breath can be used as a biomarker, or biological indicator, of those damaging processes. In other words, searching for unique VOC profiles in the breath of sarcoidosis patients might lead to the development of a diagnostic tool that only uses their exhaled breath. The current study involves 25 sarcoidosis patients and 25 healthy volunteers. The aim of this study is find VOCs in exhaled air that can be used to diagnose sarcoidosis. In a previous study, sarcoidosis-specific VOCs were found, which we intend to validate using the current study.

NCT ID: NCT02356445 Recruiting - Sarcoidosis Clinical Trials

Use of Immunosuppressive Therapy for Sarcoidosis

Start date: November 2014
Phase: N/A
Study type: Observational

Retrospective review of the outcome of use of immunosuppressive drugs in treatment of sarcoidosis

NCT ID: NCT02348905 Not yet recruiting - Sarcoidosis Clinical Trials

ACTHAR Gel for Cutaneous Sarcoidosis: An Open Label Trial

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

ACTHAR gel has efficacy in the treatment of cutaneous sarcoidosis

NCT ID: NCT02298491 Completed - CNS Sarcoidosis Clinical Trials

CNS Sarcoidosis and Acthar Gel

Start date: May 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see if treatment with H.P. Acthar® Gel will result in the improvement and long-term stabilization of clinical and radiographic abnormalities that occur in patients with CNS sarcoidosis. In addition, it will also look at whether treatment will be also associated with improvement in measures of quality of life. The treatment of CNS sarcoidosis involves the use of either corticosteroids such as prednisone or potent immunosuppressive agents such as methotrexate, both which can induce severe long term side effects. The adverse effects of steroids may be avoided by treatment with adrenocorticotropic hormone (ACTH), which is available for patient use as H.P. Acthar® Gel. The efficacies of H.P. Acthar® Gel in the treatment of CNS sarcoidosis and the impact on quality of life have not been previously studied. In addition, little is known regarding the expression of immune markers in CNS sarcoidosis and the association of such markers with disease activity and response to treatment.

NCT ID: NCT02270333 Completed - Sarcoidosis Clinical Trials

Inspiratory Muscle Training in Sarcoidosis

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

Respiratory muscle weakness results with decreased exercise capacity, worse fatigue, dyspnea and quality of life in patients with sarcoidosis. However, no study investigated the effects of inspiratory muscle training (IMT), therefore effects of IMT on outcomes in patients with sarcoidosis were investigated.

NCT ID: NCT02265874 Completed - Sarcoidosis Clinical Trials

Nicotine Treatment for Pulmonary Sarcoidosis: A Clinical Trial Pilot Study

Start date: January 12, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if nicotine treatment is beneficial for the treatment of sarcoidosis. Sarcoidosis is a disease of unknown cause that leads to inflammation. This disease affects your body's organs.

NCT ID: NCT02246023 Completed - Lung Cancer Clinical Trials

Fractionated Versus Target-controlled Propofol Administration in Bronchoscopy

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

After randomization, the subjects undergo flexible bronchoscopy either with fractionated propofol administration or with propofol-TCI. Measurement of blood pressure, heart rate, oxygen saturation, and oxygen requirement are measured continuously during the procedure and thereafter. Cumulative propofol dose, and induction, procedure, and recovery time are noted continuously during and after the procedure.

NCT ID: NCT02243995 Completed - Sarcoidosis Clinical Trials

Physical Training in Sarcoidosis Patients

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

Exercise intolerance, muscle weakness and fatigue complaints are frequent and persistent problems in sarcoidosis. These physical impairments are disabling and affect quality of life in a negative way. The aetiology of these physical impairments is multifactorial. Physical inactivity can cause deconditioning, resulting in more perceived fatigue and muscle weakness. These symptoms may be partially reversible following a structured physical training program. However, scientific studies about physical training in sarcoidosis are lacking. Therefore, the aim of the present study is to examine the changes in fatigue complaints, physical functioning and quality of life (QOL) in patients with sarcoidosis following a 13-week physical training program. After obtaining written informed consent, sarcoidosis patients will start a 13-week physical training program for three times a week. This training program includes peripheral muscle training for both the upper and lower extremities (starting at 40% of the multiple-repetition maximum) and endurance training consisting of walking on a treadmill (starting at 60% of the speed of the 6-minute walk test) or cycling on a ergometer (starting at 50% of the Wmax). Participants will be assessed at baseline (week 0), at the end (13 weeks) and 3 months after ending the training. During these assessments, patients perform muscle strength (m. quadriceps and m. biceps) and exercise tests (six-minute walk test and submaximal endurance cycling test). They also complete several questionnaires: Fatigue Assessment Scale (FAS), World Health Organization Quality of Life assessment instrument-BREF (WHOQOL-BREF), Small Fiber Neuropathy Screening List (SFNSL), Medical Research Council (MRC), Visual Analogue Scale (VAS) and Hospital Anxiety and Depression Scale (HADS)