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Pain clinical trials

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NCT ID: NCT00349921 Completed - Pain Clinical Trials

Clonidine Versus Adenosine to Treat Neuropathic Pain

Start date: August 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effects of clonidine and adenosine on nerve pain.

NCT ID: NCT00348777 Completed - Pain Clinical Trials

THERMARTHROSE: Gonarthrosis and Water Cure

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

The main objective of this study is to evaluate the therapeutic effect of a thermal treatment on gonarthrosis, with an increase of the number of patients presenting a clinically significant improvement.

NCT ID: NCT00348491 Completed - Pain Clinical Trials

Efficacy of Lumiracoxib in Relieving Moderate to Severe Post-dental Surgery Pain, Compared to Both Placebo and Celecoxib

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

This study will assess the safety and efficacy of lumiracoxib 400 mg in relieving moderate to severe post-dental surgery pain, compared to both placebo and celecoxib 400 mg.

NCT ID: NCT00345787 Completed - Pain Clinical Trials

Comparison of BTDS (Buprenorphine Transdermal System) and Placebo in Osteoarthritic Pain

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

The primary objective of this study is to evaluate the efficacy and safety of BTDS compared to placebo in subjects with moderate to severe osteoarthritic pain of the hip or knee.

NCT ID: NCT00345735 Completed - Pain Clinical Trials

Intranasal Fentanyl for the Treatment of Breakthrough Pain in Cancer Patients (FT-017-IM)

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

Primary Objective: To demonstrate the efficacy of intranasal fentanyl in the treatment of breakthrough pain (BTP) in cancer patients. Secondary Objective: To explore the relationship between the response to the fentanyl dose and the stable background pain opioid dose.

NCT ID: NCT00344045 Completed - Pain Clinical Trials

Study to Evaluate The Analgesic Efficacy and Safety of Intravenous Paracetamol in Subjects With Postoperative Pain After Total Hip Arthroplasty

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

The main purpose is to evaluate the analgesic efficacy of 1g of intravenous (Iv) paracetamol versus i.v. placebo, administered every 6h, as measured by the reduction of the 24-hour cumulative dose of the opioid tramadol in the treatment of postoperative pain following total hip arthroplasty.

NCT ID: NCT00343733 Completed - Pain Clinical Trials

Study to Evaluate the Efficacy and Safety of OraVescent Fentanyl Citrate Treatment for the Management of Breakthrough Pain in Opioid-Tolerant Patients With Noncancer-Related Chronic Pain

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

The purpose of the study is to evaluate the efficacy and safety of OraVescent fentanyl treatment compared to placebo treatment monthly over a 12-week treatment period in alleviating breakthrough pain (BTP) in opioid-tolerant patients with noncancer-related chronic pain.

NCT ID: NCT00341367 Completed - Pain Clinical Trials

Blood Sample Donations to Study the Role of Genes in Pain

Start date: December 10, 2002
Phase: N/A
Study type: Observational

This study attempts to identify genes that may increase or decrease the likelihood of sciatic pain (shooting pain down the leg) persisting 1 year after treatment of a herniated spinal disc. Many proteins in the nerves, spinal cord, and brain are involved in processing pain. These proteins vary slightly in different people. Animal studies have shown that rats and mice with certain types of proteins experience chronic pain after sciatic injury while those with other types do not. Better information about the role of genes in pain processing may lead to a test for the risk of chronic pain for specific individuals and more effective treatment approaches. This study will include people who participated in the Maine Lumbar Pain Study of the natural history of spinal pain. The Maine study included patients treated for sciatic pain caused by a herniated disc. In this study, patients who did not improve with medical treatment were referred for surgery to remove the disc. Of those referred for surgery, 275 elected to have the operation, and 232 did not. One year after surgical consultation, leg pain was reduced in 81 percent of patients who underwent surgery. Of those who declined surgery, 56 percent improved after 1 year. This study will look for genetic differences in the non-surgical group that might reveal differences among those who improved and those who did not. Participants will provide a blood sample (approximately 2 tablespoons) for genetic testing. They will also provide information on the ethnic background of their parents and grandparents. Different gene variants occur in different ethnic groups, so information on ethnic background will help researchers know what gene variants to look for. Participants will complete a questionnaire about their smoking history, because the same protein in the brain that responds to nicotine may also play a part in decreasing or increasing pain. Also, some surgeons believe that smoking can interfere with spinal bone healing. Information from this study will help resolve this question.

NCT ID: NCT00337870 Completed - Pain Clinical Trials

Painful Procedures in the Emergency Department: A Distraction Intervention (3-5 Year Olds)

ERPain
Start date: March 2006
Phase: Phase 2
Study type: Interventional

This study is designed to assess the effectiveness of the video-based intervention over and above current standard practice for pain control in the pediatric emergency department (ED). This is a single-center trial based at the IWK Health Centre. The primary outcome will be based on the Child-Adult Medical Procedures Interaction Scale (CAMPIS) coding of the video-taped pain response of the research participants (3-5 years old).

NCT ID: NCT00333918 Completed - Pain Clinical Trials

Safety/Efficacy of Bromfenac Ophthalmic Solution for Ocular Inflammation and Pain Associated With Cataract Surgery

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

The primary objective of this study is to investigate the efficacy and safety of bromfenac ophthalmic solution for treatment of ocular inflammation and pain in subjects who undergo cataract extraction and intraocular lens implantation.