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Pain clinical trials

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NCT ID: NCT00827515 Withdrawn - Pain Clinical Trials

Relative Bioavailability and Food Effect Study

Start date: February 2009
Phase: Phase 1
Study type: Interventional

Initial studies have used a powder in capsule formulation of PH797804. In future studies an immediate release tablet will be used. The purpose of this study is to compare blood levels of PH797804 following an oral dose of the powder in capsule formulation and the tablet formulation. In addition the effect of food blood levels of PH797804 will be investigated

NCT ID: NCT00769990 Withdrawn - Breast Cancer Clinical Trials

Genistein in Treating Patients Undergoing External-Beam Radiation Therapy for Bone Metastases

Start date: September 2008
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Genistein may increase the effectiveness of radiation therapy in treating pain caused by bone metastases. PURPOSE: This phase I/II trial is studying the side effects of genistein and to see how well it works in treating patients undergoing external-beam radiation therapy for pain caused by bone metastases.

NCT ID: NCT00742807 Withdrawn - Pain Clinical Trials

Pain Evaluation During Follicle Aspiration: Comparison of Two Sedation Protocols

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

Giving infiltration analgesia around the neck of the womb (= paracervical block, PCB) is frequently experienced as a painful procedure by women undergoing follicle aspiration. Two sedation protocols, where in the one protocol a low dose of alfentanil hydrochloride is already administered before the PCB, will be compared with each other and pain relief measured using the 'Visual Analogue Scale' and the 'Short-Form McGill Questionnaire'

NCT ID: NCT00737191 Withdrawn - Pain Clinical Trials

Opioids With or Without Olanzapine in Treating Patients With Moderate to Severe Cancer Pain

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

RATIONALE: Opioids lessen pain caused by cancer. It is not yet known whether opioids are more effective when given together with or without olanzapine in treating cancer pain. PURPOSE: This randomized clinical trial is studying opioids to see how well they work when given together with or without olanzapine in treating patients with moderate to severe cancer pain.

NCT ID: NCT00726791 Withdrawn - Pain Clinical Trials

Efficacy of rTMS (Repetitive Transcranial Magnetic Stimulation) on Patients With Somatoform Pain Disorder

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

Chronic somatoform pain is common in psychiatric patients. Chronic somatoform pain causes significant distress and disrupts social functioning. Moreover, chronic somatoform pain often does not sufficiently respond to medication. Chronic somatoform pain is associated with medial pain system. The medial pain system is comprised of structures engaged in affect and motivation, such as medial thalamus and limbic structures. The medial pain system gets inhibitory control from motor cortex. Functional neuroimaging studies indicate that chronic somatoform pain is associated with hypoactivity of motor cortex, defective inhibitory process, and hyperactivity of medial pain system. Repetitive Transcranial Magnetic Stimulation (rTMS) is a safe and non-invasive tool to modulate neurophysiologic activity of the focal brain. Therefore, pain relief by rTMS can be obtained from motor cortex stimulation, restoration of defective inhibitory process, and deactivation of medial pain system. Studies have shown that motor cortex stimulation using rTMS can relieve pain in patients with neuropathic pain. However, to our knowledge, there is no rTMS study on chronic somatoform pain in psychiatric patients. The purpose of this study is to evaluate the effect of motor cortex rTMS on chronic somatoform pain.

NCT ID: NCT00693043 Withdrawn - Pain Clinical Trials

Pilot Study About Safety and Efficacy of Atomized Intrapleural Lidocaine During Pleuroscopy

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

This study will evaluate the potential to decrease the use of IV anesthesia drugs in patients undergoing pleuroscopy administering lidocane standardly applied to the skin in combination with atomized lidocaine applied into the pleural cavity.

NCT ID: NCT00691886 Withdrawn - Pain Clinical Trials

Safety and Efficacy of Intravenous (IV) Dexmedetomidine During Flexible Bronchoscopy and Endobronchial Ultrasound

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

To achieve safe,consistent, continuous sedation using Dexmedetomidine in advaced bronchoscopy procedures that may reduce the need for rapid pain sedative infusion.

NCT ID: NCT00678548 Withdrawn - Pain Clinical Trials

Effect of Guided Imagery on Patients With Chronic Pain Related to Spinal Cord Injury

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

Chronic pain after spinal cord injury in or below the level of injury is a common problem and can be severe. The purpose of our study is to investigate the effect of pleasant guided imagery on spinal cord injured patients with chronic pain in or below the level of injury.

NCT ID: NCT00676000 Withdrawn - Pain Clinical Trials

Randomized Trial of Interrupted Versus Continuous Vaginal Closure of Anterior Repair With Mesh

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

Vaginal prolapse is a common condition that is treated with surgical correction. Recently surgeons have been using mesh to augment the repair of vaginal prolapse. Common complications of this surgery include vaginal pain, pain during sex, infection or erosion of the mesh in the vagina. There are different ways to close the vaginal wall over the mesh used in these procedures. Currently, there is no accepted standard method of closing the vaginal wall. The purpose of this study is to find out the best way to close the surgical wound in the vagina. We will compare interrupted closure (separate stitches) to continuous closure (one long, running stitch). We hope to show in our study that one method of closure is better than the other.

NCT ID: NCT00667238 Withdrawn - Pain Clinical Trials

Chronic Pediatric Pain

Start date: November 1, 2008
Phase:
Study type: Observational

The purpose will be to study the functional impact of pediatric chronic pain on children, and their families. Focus will be on the impact of pain on school functioning, social functioning, psychological functioning and family functioning of pediatric chronic pain.