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Pain, Intractable clinical trials

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NCT ID: NCT00866164 Approved for marketing - Back Pain Clinical Trials

Prometra's Utilization in Mitigating Pain II

(PUMP 2)
Start date: n/a
Phase: N/A
Study type: Expanded Access

Intrathecal infusion pumps are increasingly used to deliver analgesics for chronic intractable pain. The PUMP II trial is designed to evaluate the ongoing safety and efficacy of the new Prometra® Programmable Pump System for intrathecal administration of morphine sulfate to treat chronic intractable pain.

NCT ID: NCT00817596 Completed - Intractable Pain Clinical Trials

Prometra's Utilization in Mitigating Pain (PUMP)

PUMP
Start date: January 2007
Phase: N/A
Study type: Interventional

Clinical evaluation of the safety and efficacy of the Prometra Programmable Infusion Pump to accurately supply drug to the intrathecal space for the treatment of chronic pain.

NCT ID: NCT00804154 Recruiting - Palliative Care Clinical Trials

Resiniferatoxin to Treat Severe Pain Associated With Advanced Cancer

Start date: August 14, 2009
Phase: Phase 1
Study type: Interventional

This study will examine the safety of giving the experimental drug, resiniferatoxin (RTX), to treat severe pain in patients with advanced cancer. RTX is a chemical extracted from a cactus-like plant. It is similar to capsaicin, the active ingredient in hot pepper. RTX has relieved pain and reduced the need for pain medication in several animal experiments. It works by destroying nerves that transmit pain information. People at least 18 years of age with severe pain from advanced cancer at or below the level of the chest that cannot be controlled with standard treatments may be eligible for this study. Participants undergo the following procedures: Pretreatment Visit Before beginning treatment with RTX, patients give a medical history and undergo a physical examination that includes: - Electrocardiogram (EKG) - Blood draw - Urinalysis - Neurological examinations - Peak expiratory flow rate (PEFR) - Eye examination - MRI - Urology assessment - Pregnancy test, when appropriate - Questionnaires to collect information on health, personality, mood, pain levels and symptoms. 2-Day Hospitalization Patients are hospitalized for 2 days for RTX injection and monitoring, as follows: - RTX injection: RTX is injected in the operating room under general anesthesia. It is given through a catheter placed in the patient s spine. The catheter is also used to obtain samples of cerebrospinal fluid (CSF) the clear fluid that bathes the spinal cord. The fluid is examined to assess drug effects and side effects, chemical changes in the content of the CSF associated with RTX, and how RTX is handled by the body. - Post-injection monitoring, including: - Surveys about symptoms such as pain or weakness - Neurological examinations - Blood and CSF sampling - EKG - AEs Outpatient followup - Vitals - Blood draw, Urinalysis, neurological and sensory testing, EKG on days 7, 14 and 30 after the injection - MRI scans of the head and back, Urology assessment and PEFR on day 15 after the injection - Eye examination - Follow-up phone calls monthly for 6 months

NCT ID: NCT00552578 Terminated - Opiate Addiction Clinical Trials

Buprenorphine as a Treatment in Opiate Dependent Pain Patients

Start date: October 2007
Phase: Phase 4
Study type: Interventional

This study is designed to determine if different doses of buprenorphine (either tapering doses or steady doses) are effective in managing chronic, non-cancer pain in individuals who also are addicted to opiate pain medicines.

NCT ID: NCT00414466 Terminated - Clinical trials for Chronic Intractable Pain

A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Treatment of Chronic Pain

Start date: December 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and minimum effective dose of intraspinal gabapentin when delivered through an implanted drug infusion system.

NCT ID: NCT00387244 Terminated - Pain Clinical Trials

Efficacy of the Spinal Cord Stimulation System as Salvage Therapy

Start date: August 2006
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the efficacy of spinal cord stimulation using the Precision implantable neurostimulation device for chronic and intractable pain of the trunk and or limbs in patients who have failed treatment with an intraspinal infusion pump or other SCS system.

NCT ID: NCT00386243 Completed - Pain Clinical Trials

Evaluation of Stepped Care for Chronic Pain in Iraq/Afghanistan Veterans (ESCAPE)

ESCAPE
Start date: December 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a stepped-care intervention makes pain symptoms better and reduces activity limitations because of pain. Our two primary hypotheses are that in OIF/OEF veterans with chronic pain: 1. Stepped care is more effective than usual care in reducing pain-related disability 2. Stepped care is more effective than usual care in reducing psychological distress

NCT ID: NCT00381095 Terminated - Cancer Clinical Trials

A Study To Evaluate Pregabalin In The Treatment Of Moderate To Severe Chronic Bone Pain Related To Metastatic Cancer

COPE
Start date: December 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the analgesic efficacy of flexibly-dosed pregabalin in the adjunctive treatment of subjects with cancer-induced bone pain.

NCT ID: NCT00371865 Completed - Intractable Pain Clinical Trials

Behavioral Treatments for Chronic Pain

Start date: October 2006
Phase: N/A
Study type: Interventional

The purpose of the study is to test a brief, group-administered psychosocial intervention to reduce interference of pain with daily life, emotional distress, and pain intensity, and improve quality of life and physical activity levels in individuals with chronic pain.

NCT ID: NCT00321347 Withdrawn - Pain Clinical Trials

Intravenous (IV) Lidocaine for Opioid-refractory Pain

Start date: May 2006
Phase: Phase 2
Study type: Interventional

Opioid medicines, like morphine, are the main treatment for severe cancer pain. Unfortunately, some patients suffer severe pain despite high doses of opioids. We hypothesize that intravenous lidocaine can quickly and effectively treat this kind of opioid-refractory pain.