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Neuralgia clinical trials

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NCT ID: NCT00629681 Completed - Clinical trials for Painful Diabetic Neuropathy and Post Herpetic Neuralgia

A Study of the Efficacy and Safety of Pregabalin for the Treatment of Diabetic Peripheral Neuropathy or Postherpetic Neuralgia

Start date: November 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of pregabalin for the treatment of diabetic peripheral neuropathy (DPN) or postherpetic neuralgia (PHN)

NCT ID: NCT00623961 Completed - Clinical trials for Diabetic Peripheral Neuropathy

Validation Study of Neuropathic Pain

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

This study seeks to validate clinically evoked or obtained objective pain signs with the patient's corresponding quantified subjective pain symptoms. This will allow for validation of objective clinical pain signs to then be used to begin to classify patients with pain based on symptoms and signs. This then can be used as a basis for further study of neuropathic pain mechanisms in human patients.

NCT ID: NCT00619476 Completed - Clinical trials for Neuralgia, Postherpetic

A Study In Patients With Neuropathic Pain From Post-Herpetic Neuralgia (PHN)

Start date: February 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether gabapentin enacarbil (XP13512/GSK1838262), hereafter referred to as GEn is effective in the treatment of neuropathic pain associated with post-herpetic neuralgia (PHN).

NCT ID: NCT00617461 Completed - Clinical trials for Neuralgia, Postherpetic

A Clinical Study in Subjects With Neuropathic Pain From PHN Who Have Had an Inadequate Response to Gabapentin Treatment

Start date: March 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is evaluate the difference between two doses of gabapentin enacarbil (XP13512/GSK1838262), hereafter referred to as GEn, on pain associated with post-herpetic neuralgia.

NCT ID: NCT00614705 Completed - Clinical trials for Neuralgia, Postherpetic

PH-797804 Versus Placebo For The Treatment Of Neuropathic Pain Associated With Post-Herpetic Neuralgia

Start date: April 2008
Phase: Phase 2
Study type: Interventional

This is a proof-of-concept study to determine if PH-797804 reduces neuropathic pain associated with post-herpetic neuralgia. Suitable patients will be randomized to receive either PH-797804 or placebo for 4 weeks, during which time they will also record their pain symptoms using various pain scales.

NCT ID: NCT00612105 Completed - Clinical trials for Postherpetic Neuralgia

Safety/Efficacy Study of Retigabine vs. Placebo in Post-Herpetic Neuralgia (PHN)

Start date: October 2007
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the efficacy of retigabine vs. placebo in reducing pain associated with post-herpetic neuralgia.

NCT ID: NCT00611949 Completed - Neuropathic Pain Clinical Trials

Comparison of 2 Vials of Components of a Synthetic Geranium Oil

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

The purpose of this study is to determine which component of an artificial geranium oil helps to reduce your neuropathy pain.

NCT ID: NCT00610155 Completed - Pain Clinical Trials

A Methodology Study Of Brain Imaging Of Pain-Killers In Post-Traumatic Neuropathic Pain Patients

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

This study is a methodology study designed to discover whether a brain imaging technology is a better way of compare the relative sensitivities of fMRI and subjective psychometric assessments of pain to multiple doses of pregabalin and tramadol SR in a cross-over clinical study design.

NCT ID: NCT00609323 Completed - Clinical trials for Postherpetic Neuralgia

Lidocaine and Tetracaine Cream to Treat Postherpetic Neuralgia (PHN)

Start date: January 2008
Phase: Phase 2
Study type: Interventional

Pliaglis™ (lidocaine and tetracaine) Cream 7%/7% is a topical local anesthetic cream that forms a pliable peel on the skin when exposed to air. When applied to intact skin, Pliaglis provides local dermal analgesia by the release of lidocaine and tetracaine from the peel into the skin. Pliaglis is currently approved in the United States for use on intact skin in adults to provide topical local analgesia for superficial dermatological procedures such as dermal filler injection, pulsed dye laser therapy, and facial laser resurfacing. This study will evaluate lidocaine and tetracaine cream 7%/7% for the treatment of pain associated with postherpetic neuralgia (PHN).

NCT ID: NCT00603265 Completed - Neuropathic Pain Clinical Trials

Safety and Efficacy Study of ADL5859 in Participants With Neuropathic Pain Associated With Diabetic Peripheral Neuropathy

Start date: November 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of ADL5859 in relieving the pain associated with diabetic peripheral neuropathy (DPN) compared with placebo and duloxetine (a marketed drug approved for the treatment of painful DPN). The pain symptoms of DPN are thought to be due to damage to nerves caused by the diabetes.