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Pain clinical trials

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NCT ID: NCT00902733 Completed - Pain Clinical Trials

Nurse-Provided Care or Standard Care in Treating Patients With Pancreatic Cancer

Start date: July 2008
Phase: N/A
Study type: Interventional

RATIONALE: Meeting with a nurse to assess symptoms and quality of life may be more effective than standard care in treating patients with pancreatic cancer. PURPOSE: This clinical trial is studying nurse-provided care to see how well it works compared with standard care in treating patients with pancreatic cancer.

NCT ID: NCT00902642 Completed - Pain Clinical Trials

What is the Effect of a Course for Treatment Providers on Their Patient Outcome

Start date: September 2004
Phase: N/A
Study type: Interventional

The goal is to acquire more in-depth knowledge on physical therapists' attitudes towards and beliefs about psychosocial factors in back pain, how physical therapists integrate psychosocial factors into their clinical practice and the effects of a training program for physical therapists in psychosocial factors on clinical practice and thereby on patient outcome in terms of disability, pain, catastrophizing, and treatment satisfaction.

NCT ID: NCT00902330 Completed - Breast Cancer Clinical Trials

Cranial Stimulation for Chemotherapy Symptoms in Breast Cancer

Start date: April 2009
Phase: Phase 3
Study type: Interventional

RATIONALE: Cranial microcurrent electrical stimulation (CES) is mild electrical current received through electrodes placed on the earlobes. CES may lessen symptoms in women with breast cancer receiving chemotherapy. It is not yet known whether CES is more effective than sham therapy in reducing symptoms caused by chemotherapy in women with breast cancer. PURPOSE: This randomized phase III trial is studying mild electrical stimulation to see how well it works compared with sham therapy in reducing symptoms caused by chemotherapy in women with stage I, stage II, or stage IIIA breast cancer receiving chemotherapy.

NCT ID: NCT00900835 Completed - Breast Cancer Clinical Trials

Pain and Fatigue Management in Patients With Breast Cancer, Prostate Cancer, Colon Cancer, or Lung Cancer

Start date: June 2005
Phase: N/A
Study type: Interventional

RATIONALE: Collecting information over time about patients' and health care providers' understanding of pain and fatigue and providing education about pain and fatigue management may improve quality of life. PURPOSE: This clinical trial is studying pain and fatigue management in patients with breast cancer, prostate cancer, colon cancer, or lung cancer.

NCT ID: NCT00895869 Completed - Pain Clinical Trials

Pain in Neonates During Screening for Retinopathy of Prematurity Using Two Methods

RETCAM
Start date: April 2004
Phase: N/A
Study type: Observational

Retinopathy of prematurity screening is painful. Wide field digital retinal imaging (WFDRI) and binocular indirect ophthalmoscopy (BIO) are being used for screening examinations. The aim of Edinburgh, UK based study is to compare the pain experienced by infants using both examination techniques.

NCT ID: NCT00894699 Completed - Pain Clinical Trials

A Study to Evaluate the Clinical Efficacy, Safety and Tolerability of ARX-F03 Sublingual Sufentanil/Triazolam NanoTabâ„¢ in Patients Undergoing an Elective Abdominal Liposuction Procedure

Start date: June 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of a study medication that contains a combination of a pain medication, sufentanil, and a sedative, triazolam. This drug is being designed to provide mild sedation as well as reduce anxiety and pain before and during a procedure (in this case elective abdominal liposuction).

NCT ID: NCT00893412 Completed - Pain Clinical Trials

Fast-Release Orodispersible Tramadol Tablet (Tradonal Odis®) as Analgesia for Hysterosalpingography

Start date: November 2008
Phase: Phase 4
Study type: Interventional

This study evaluates the analgetic effects of the fast-release orodispersible tramadol tablet. Tramadol acts through a weak affinity for μ receptors and secondly by inhibiting noradrenaline and serotonin neuronal reuptake. It has been used since the 1970s by over 50 million people for the treatment of acute and chronic pain. The orodispersible Tramadol tablet is a new galenic form and is available on the Belgian market for the last three years. Pregastric absorption leads to a quicker onset of action. So far, evidence shows that pain during and immediately after the Hysterosalpingography (HSG) procedure is only significantly reduced by IV opioid analgesia. This study evaluates the analgetic potential of an orodispersible opioid tablet. This tablet disintegrates rapidly (in around 20-30 seconds) and may be taken without water. Its abuse potential is very low and its respiratory depressant effect is negligible.

NCT ID: NCT00893100 Completed - Pain Clinical Trials

Evaluation of Pain Reduction After Hemorrhoidectomy With Use of Diltiazim Ointment 2%

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

The purpose of this study is to evaluate the effectiveness of diltiazem ointment 2 percent in reducing pain after hemorrhoidectomy.

NCT ID: NCT00891163 Completed - Pain Clinical Trials

Evaluate the Depth and Duration of Anesthesia

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

The purpose of the study is to determine the depth (mm) of anesthesia provided by the Synera topical patch (using sensory depth and pain depth evaluations), and to determine the duration (minutes) of anesthesia provided by the Synera topical patch (using dermal sensory testing and thermal sensory testing evaluations), compared with a matching heated placebo patch.

NCT ID: NCT00889499 Completed - Pain Clinical Trials

Modulation of Central Hypersensitivity in Chronic Musculoskeletal Pain by Intravenous Tropisetron

Start date: March 2009
Phase: Phase 2
Study type: Interventional

Chronic pain is associated with hypersensitivity of the central nervous system. The drug under investigation (tropisetron) has been shown in animal studies to attenuate central hypersensitivity. It has therefore the potential to be effective in chronic pain. We compare two doses of tropisetron with placebo in patients with chronic pain. We measure pain intensity and parameters that assess central hypersensitivity.