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Pain clinical trials

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NCT ID: NCT00482560 Completed - Pain Clinical Trials

Analgesic Effect of Breast Feeding vs Sucrose in Neonatal Screening

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

The purpose of this study is to compare the antinociceptive effect of 1 ml of 30% sucrose solution vs breastfeeding on neonatal screening heel lance

NCT ID: NCT00482378 Completed - Pain Clinical Trials

Samarium Sm 153 Lexidronam Pentasodium Combined With Zoledronic Acid or Pamidronate in Treating Patients With Relapsed or Refractory Multiple Myeloma and Bone Pain

Start date: March 21, 2005
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Radioactive drugs, such as samarium Sm 153 lexidronam pentasodium, may carry radiation directly to cancer cells and not harm normal cells. Zoledronic acid and pamidronate may help relieve bone pain caused by multiple myeloma. Giving samarium Sm 153 lexidronam pentasodium together with zoledronic acid or pamidronate may be an effective treatment for multiple myeloma. PURPOSE: This phase I/II trial is studying the side effects and best dose of samarium Sm 153 lexidronam pentasodium when given together with zoledronic acid or pamidronate and to see how well it works in treating patients with relapsed or refractory multiple myeloma and bone pain.

NCT ID: NCT00478179 Completed - Pain Clinical Trials

Study of a Bupivacaine Patch (Eladurâ„¢) to Treat Post- Herpetic Neuralgia

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

Neuropathic pain is caused by a virus commonly associated with chicken pox. This virus may become dormant in the nervous system and later reactivate causing herpes zoster, also known as "shingles". Post-herpetic neuralgia (PHN) is a persistent pain in the area of healed skin lesions. This study will test the safety and efficacy of treating PHN patients with the analgesic patch, Bupivacaine TTS (Eladurâ„¢).

NCT ID: NCT00474721 Completed - Pain Clinical Trials

Comparison of Acetaminophen With Codeine and Ibuprofen for Children With Injuries

Start date: November 2002
Phase: N/A
Study type: Interventional

We compared the pain relief of acetaminophen with codeine versus ibuprofen for children ages 5-18 years who came to the Pediatric Emergency Department with injuries to their arms or legs.

NCT ID: NCT00472303 Completed - Pain Clinical Trials

A Study to Evaluate Tapentadol (CG5503) in the Treatment of Chronic Tumor-Related Pain Compared With Placebo and Morphine

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

The purpose of this study will be to determine whether tapentadol (CG5503) is effective and safe in the treatment of chronic tumor related pain compared to placebo. In addition tapentadol (CG5503) will also be compared to morphine controlled release, also referred to as slow release (SR). *Tapentadol prolonged-release (PR) is the term used in the European Union and is referred to as extended release (ER) in the United States.

NCT ID: NCT00471445 Completed - Pain Clinical Trials

Topical Amitriptyline and Ketamine Cream in Treating Peripheral Neuropathy Caused by Chemotherapy in Cancer Patients

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

RATIONALE: Topical cream containing amitriptyline and ketamine may help relieve pain, numbness, tingling, and other symptoms of peripheral neuropathy. It is not yet known whether topical amitriptyline and ketamine cream is more effective than a placebo in treating peripheral neuropathy caused by chemotherapy. PURPOSE: This randomized phase III trial is studying the side effects and how well topical amitriptyline and ketamine cream work compared with a placebo in treating peripheral neuropathy caused by chemotherapy in patients with cancer.

NCT ID: NCT00470652 Completed - Pain Clinical Trials

Management of Acute Pain in the Emergency Department

Start date: May 2007
Phase: N/A
Study type: Observational

Oligoanalgesia1 has been widely recognized as an issue in emergency department.The purpose of our study is to assess the impact of the implementation of a computer-assisted support program to improve pain management in our ED.

NCT ID: NCT00470600 Completed - Pain Clinical Trials

Efficacy and Safety Study of Caldolor (IV Ibuprofen) in Hospitalized Adult Orthopedic Patients

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

The primary objective of this study of Caldolor (IV ibuprofen) administered to post-operative hospitalized adult orthopedic patients every 6 hours for at least 24 hours is to determine the efficacy of Caldolor (IV ibuprofen) compared to placebo for the treatment of post-operative pain by patients self-assessment of pain.

NCT ID: NCT00470080 Completed - Pain Clinical Trials

Randomised Trial of Eutectic Mixture of Local Anaesthetics Cream and Oral Sucrose Solution for Venepuncture

VIEP
Start date: June 2007
Phase: Phase 4
Study type: Interventional

This randomized bicentric trial will investigate the efficacy of topical EMLA cream with oral sucrose solution compared to oral sucrose solution alone before venepuncture in preterm infants.

NCT ID: NCT00466830 Completed - Breast Cancer Clinical Trials

Psychological and Social Factors That May Increase the Risk of Developing Chronic Pain After Surgery in Women With Breast Cancer

Start date: September 2005
Phase: N/A
Study type: Observational

RATIONALE: Certain psychological and social factors may increase the risk of developing chronic pain after surgery. Evaluating these factors over time in patients who have undergone surgery for breast cancer may help doctors plan treatment and improve patients' quality of life. PURPOSE: This clinical trial is studying the psychological and social factors that may increase the risk of developing chronic pain after surgery in women with breast cancer .