Status | Study |
Completed |
Study Name: rTMS as a Treatment of Visceral Pain Secondary to Malignancy Condition: Malignancy Date: 2014-03-19 Interventions: Procedure: Real rTMS(20 Hz, 10 trains, inter train interval 30 sc with total |
Withdrawn |
Study Name: Compounded Pain Creams and Patient Perception Condition: Neurologic Pain Nociceptive Pain Date: 2013-12-28 |
Completed |
Study Name: The Post-operative Analgesia of the Virtual Reality Using a Mirror Therapy After Total Knee Arthroplasty Condition: Osteoarthritis, Knee Nociceptive Pain Date: 2013-11-03 Interventions: Device: Mirrored Virtual reality Patients are required to look at the images of both lower extremities r |
Completed |
Study Name: A Phase 2a, Proof-of-Concept Study of GIC-1001 in the Management of Visceral Pain During Sedation-Free, Full Colonoscopy Condition: Pain Cancer Colonic Diseases Date: 2013-08-08 Interventions: Drug: GIC-1001 GIC-1001 oral tablet, white-coated, to be taken with water |
Withdrawn |
Study Name: tDCS for the Management of Chronic Visceral Pain in Patients With Chronic Pancreatitis Condition: Chronic Pancreatitis Pain Date: 2013-05-16 Interventions: Device: tDCS Other Name: Soter |
Active, not recruiting |
Study Name: Neuroimaging and Biomarkers in Chronic Visceral Pain Condition: Irritable Bowel Syndrome Date: 2012-05-17 Interventions: Behavioral: Mindfulness based Stress Reduction Training (MBSR) 8 (2 hr) classes weekly of MBSR and requi |
Completed |
Study Name: Determine the Effect of AZD3161,Injected Intradermally, on Quantitative Sensory Testing Variables in Normal and Ultraviolet-C (UVC) Exposed Skin in Healthy Volunteers Condition: Peripheral Neuropathic Pain Nociceptive Pain Date: 2010-11-10 Interventions: Drug: AZD3161 Single dose, int |
Completed |
Study Name: Development of a Questionnaire to Measure Hypervigilance for Visceral Pain Condition: Irritable Bowel Syndrome Date: 2010-07-19 |
Completed |
Study Name: Lubiprostone Effects on Visceral Pain Sensitivity Condition: Irritable Bowel Syndrome Date: 2010-07-19 Interventions: Drug: Lubiprostone 48ug daily |
Terminated |
Study Name: Evaluation of Effectiveness and Tolerability of Tapentadol Hydrochloride in Subjects With Severe Chronic Low Back Pain Taking WHO Step III Analgesics But Showing a Lack of Tolerability Condition: Pain Chronic Pain Low Back Pain Date: 2009-09-28 Interventions: Drug: Tapentadol Prolonged Release Participants started wi |