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Pain clinical trials

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NCT ID: NCT00458796 Terminated - Breast Cancer Clinical Trials

Comparison of Two Schedules of Zoledronic Acid in Treating Patients With Breast Cancer That Has Spread to the Bone

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

RATIONALE: Zoledronic acid may help decrease the risk of broken bones, bone pain, and other symptoms caused by bone metastases. It may also help patients live more comfortably. PURPOSE: This randomized clinical trial is studying different schedules of zoledronic acid to compare how well they work in treating patients with breast cancer that has spread to the bone.

NCT ID: NCT00450905 Terminated - Pain Clinical Trials

Pain Relief Investigation of Neuromodulation Therapy in an Adult Fibromyalgia Population

Start date: March 2007
Phase: Phase 3
Study type: Interventional

This study is being performed to determine the safety and efficacy of Fralex Neuromodulation Therapy (F-NMT), delivered by the Fralex PRIMA device, in reducing chronic musculoskeletal pain associated with Fibromyalgia.

NCT ID: NCT00444808 Terminated - Pain Clinical Trials

Analgesic Effect of Intranasal Calcitonin on Patients With Fractured Ribs

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

This study, which will be conducted at the emergency room of the Sacré-Cœur hospital, requires the recruitment of 60 subjects and involves some telephone follow-up. Calcitonin administered as an intranasal spray is already used to relieve pain caused by broken vertebrae and we seek to determine if it can be as efficient in the case of pain caused by broken ribs.This study aims at testing the hypothesis that subjects suffering from the accidental fracture of one or more ribs will get relief through the intranasal spraying of calcitonin and/or will use less opiate medication for pain relief (a combination of oxycodone chlorhydrate and acetaminophen called Percocet®).

NCT ID: NCT00423241 Terminated - Pain Clinical Trials

SEMPERFLO* Pain Management System in Inguinal Hernia Repair

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

This study will compare the clinical performance of the SEMPERFLO* Pain Management System with another commercial pain relief system using 0.5% bupivacaine following unilateral, open, inguinal hernia repair procedures. *Trademark

NCT ID: NCT00403780 Terminated - Pain Clinical Trials

Randomized Study of Pregabalin for Pain Reduction in Patients With Rest Pain and Lower Limb Ischemia

Start date: June 2006
Phase: Phase 4
Study type: Interventional

The hypothesis behind the trial is the concept that Pregabalin is effective in reducing pain at rest in lower limb ischemia, and the study evaluates active treatment or placebo added to the regular pain regimens for these patients.

NCT ID: NCT00399841 Terminated - Pain Clinical Trials

Spinal Cord Stimulation (SCS) for Neuropathic Pain of Back or Lower Extremity

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

The primary objective of this study is to compare the efficacy and patient preference for spinal cord stimulation (SCS) using the Precision device with the electrode array placed at T7 versus placement at T8. Eligible patients will have chronic intractable pain in the back or lower extremities and will have independently elected SCS as the next line of therapy. There is some anecdotal evidence that the coverage of the paresthesia resulting from T7 placement is preferable to that obtained by the more commonly used T8 placement but there has been no study to support this observation.

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: NCT00387010 Terminated - Pain Clinical Trials

Open-Label Study to Evaluate the Effect of Treatment With Fentanyl Buccal Tablets on Pain Anxiety Symptoms When Used for the Management of Breakthrough Pain

Start date: December 2006
Phase: Phase 3
Study type: Interventional

The primary purpose of the study is to evaluate the impact of treatment with fentanyl buccal tablets on the anxiety symptoms commonly associated with chronic pain in patients with breakthrough pain (BTP). Other purposes are to assess the management of BTP, to evaluate patient functioning, and to determine any influences on the successful dose achieved.

NCT ID: NCT00371462 Terminated - Obesity Clinical Trials

PDA+: A Personal Digital Assistant for Obesity Treatment

PDA+
Start date: October 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether including a PDA decision support tool plus distance support enhances the outcomes attainable by the MOVE2! (Managing Obesity for Veterans Everywhere) standard care alone. Primary hypotheses are that obese patients with chronic pain who are randomized to MOVE2! + PDA + Support will a) lose more weight by 6 months, b) show greater maintenance of weight loss at 12 months, and c) display greater reduction in pain intensity and pain-related disability than those randomized to Standard Care. Secondary hypotheses are that MOVE2! + PDA + Support, compared to Standard Care will result in: a) improved quality of life, b) greater treatment adherence, and c) reduced care utilization.

NCT ID: NCT00360971 Terminated - Pain Clinical Trials

Palifermin in Lessening Oral Mucositis in Patients Undergoing Radiation Therapy and Chemotherapy for Locally Advanced Head and Neck Cancer

Start date: July 2006
Phase: Phase 3
Study type: Interventional

RATIONALE: Growth factors, such as palifermin, may lessen the severity of mucositis, or mouth sores, in patients receiving radiation therapy and chemotherapy for head and neck cancer. It is not yet known whether palifermin is more effective than a placebo in lessening mucositis in patients receiving radiation therapy and chemotherapy for head and neck cancer. PURPOSE: This randomized phase III trial is studying palifermin to see how well it works compared to a placebo in lessening oral mucositis in patients undergoing radiation therapy and chemotherapy for locally advanced head and neck cancer.