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Syndrome clinical trials

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NCT ID: NCT02800720 Completed - Clinical trials for Fibromyalgia Syndrome

Meditation Awareness Training for the Treatment of Fibromyalgia Syndrome

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

A Randomised Controlled Trial to evaluate the effectiveness of a Second-Generation Mindfulness-Based Intervention known as Meditation Awareness Training (MAT) for treating fibromyalgia syndrome.

NCT ID: NCT02800681 Completed - Clinical trials for Autism Spectrum Disorder

Psychopathological Differences Between Asperger Syndrome and Schizotypal Disorder in an Adult Sample

Start date: June 2016
Phase:
Study type: Observational

The purpose of this study is to identify psychopathology (psychiatric symptoms) that can differentiate between Schizotypal Disorder (SD) and Asperger Syndrome (normal IQ, no language impairment Autism Spectrum Disorder) (AS) in young adults. With our present knowledge, the differentiation between AS and SD can be difficult, as they both present with social difficulties, odd (but not psychotic) behaviour, and a 'feeling of not being as everyone else'. Studies suggest that adults with AS symptoms are either overlooked, or diagnosed within the schizophrenia spectrum in Adult Psychiatry. A 'correct' diagnosis is important, as it is the first step towards the most optimal plan, treatment and rehabilitation for the patient. The only way to diagnose psychiatric illness is the description of present psychopathology. To identify symptoms that can differentiate between the two disorders, we will use semi-structured interviews to explore present psychopathology in young adults with typical symptoms of SD and AS respectively, with special focus on presence of alterations in self-experience. Alterations in self-experience are typical for the schizophrenia spectrum, and are therefore not thought to be equally present in AS and SD. The hypotheses are that the total level of altered experiences is higher in SD, than in AS, and with a different pattern of altered experiences in SD than in AS. If the hypotheses are true, an examination of altered self-experience will be valuable to aid clinical differentiation between the two disorders.

NCT ID: NCT02800200 Completed - Clinical trials for Carpal Tunnel Syndrome

The Effect of Combined PRP and ESWT for Carpal Tunnel Syndrome

Start date: June 16, 2016
Phase: N/A
Study type: Interventional

The platelet rich plasma (PRP) and extracorporeal shock wave therapy (ESWT) are new and potential treatment for patients with kinds of musculoskeletal disorders. Although few clinical studies have showed beneficial effect of PRP and ESWT for regeneration of peripheral neuropathy, the effect of combined PRP and ESWT is absent so far.

NCT ID: NCT02800187 Completed - Clinical trials for Carpal Tunnel Syndrome

The Dose Effect of Extracorporeal Shock Wave Therapy in Patients With Carpal Tunnel Syndrome

Start date: April 2016
Phase: N/A
Study type: Interventional

The shock wave is a new and potential intervention for the reinnervation of peripheral nerve. The purpose of this study was to assess the dose effect of extracorporeal shock wave therapy on carpal tunnel syndrome.

NCT ID: NCT02799940 Completed - Clinical trials for Respiratory Distress Syndrome, Adult

Abnormalities in Lung Computed Tomography and Physiological Alterations in Patients With Acute Respiratory Distress Syndrome

Start date: August 2016
Phase:
Study type: Observational [Patient Registry]

The objective of the study is to determine the correlation between the physiological variables and the degree of consolidation in lung computed tomography in patients with acute respiratory distress syndrome

NCT ID: NCT02796092 Completed - Clinical trials for Pelvic Congestion Syndrome

Fibered Platinum Coils vs Vascular Plugs in Pelvic Varices Embolization for the Treatment of Pelvic Congestion Syndrome

Start date: February 2014
Phase: N/A
Study type: Interventional

This prospective randomized study compares the safety and efficacy of two different embolizing agents for the treatment of pelvic congestion syndrome: fibered platinum coils and vascular plugs.

NCT ID: NCT02794493 Completed - Hand Foot Syndrome Clinical Trials

Treatment of Hand and Foot Syndrome With Traditional Chinese Medicine Formula LC09 in Patients Who Are Receiving Capecitabine for Colorectal and/or Breast Cancer

Start date: April 1, 2015
Phase: Phase 3
Study type: Interventional

RATIONALE: Hand foot syndrome may be treated or reduced by soaking Traditional Chinese Medicine Formula LC09 in patients receiving capecitabine for colorectal and/or breast cancer. PURPOSE: This randomized phase III trial is studying soaking Traditional Chinese Medicine Formula LC09 to see how well they work compared to placebos in preventing hand-foot syndrome in patients who are receiving capecitabine for colorectal or breast cancer.

NCT ID: NCT02794376 Completed - Clinical trials for Irritable Bowel Syndrome

Mindfulness for Irritable Bowel Syndrome

MIBS
Start date: April 14, 2016
Phase: N/A
Study type: Interventional

This study investigates the effectiveness of a 6 week mindfulness intervention in reducing symptoms of Irritable Bowel Syndrome (IBS). All Participants will receive treatment. Participants will be randomly allocated to an immediate treatment group and a waiting list control group.

NCT ID: NCT02792790 Completed - Clinical trials for Carpal Tunnel Syndrome

Carpal Tunnel Syndrome and Amyloid Cardiomyopathy

Start date: March 2016
Phase:
Study type: Observational

The investigators will prospectively evaluate tissue samples obtained from patients undergoing carpal tunnel release surgery for amyloid in the soft tissue that is removed. Patients who have tissue that stains positive for amyloid will undergo cardiac testing to look for evidence of cardiac involvement.

NCT ID: NCT02791698 Recruiting - Cushing Syndrome Clinical Trials

The Accuracy of Late Night Urinary Free Cortisol/Creatinine and Hair Cortisol in Cushing's Syndrome Diagnosis

Start date: June 2016
Phase:
Study type: Observational

The investigators will conduct a prospective study, in which they will determine sensitivity, specificity and diagnostic accuracy of late evening urinary free cortisol concentration/creatinine and hair cortisol in differentiating Cushing's syndrome from Pseudo-Cushing's syndrome.