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Post-Herpetic Neuralgia clinical trials

View clinical trials related to Post-Herpetic Neuralgia.

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NCT ID: NCT03765697 Completed - Clinical trials for Post Herpetic Neuralgia

A Study With Lidocaine 5% Medicated Plaster in Patients Suffering From Postherpetic Neuralgia

Start date: July 16, 2003
Phase: Phase 3
Study type: Interventional

This study was performed to evaluate the local and systemic safety profile and the analgesic efficacy of long-term treatment with lidocaine 5% medicated plaster (Lido-Patch). The study was an open-label, multi-center, multiple-dose, Phase III study and comprised a main and an extension period. 161 participants who completed treatment in KF10004/01 (NCT03745404) and 98 newly recruited participants were enrolled.

NCT ID: NCT03745404 Completed - Clinical trials for Post Herpetic Neuralgia

A Study With Lido-Patch and Placebo Plaster in Patients Suffering From Postherpetic Neuralgia (PHN)

Start date: April 29, 2003
Phase: Phase 3
Study type: Interventional

This study investigated the efficacy of the Lido-Patch (lidocaine 5% medicated plaster) in treatment of pain caused by PHN which is a neuropathic pain syndrome (nerve-related pain conditions) following an acute attack of herpes zoster (shingles).

NCT ID: NCT03584061 Completed - Herpes Zoster Clinical Trials

Treatment of Chronic Postherpetic Pain With Fat Grafting

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

This study evaluates the possible beneficial effect of fat grafting for post herpetic neuralgia.

NCT ID: NCT03447756 Completed - Clinical trials for Diabetic Peripheral Neuropathy

Titration Study of ABX-1431

Start date: October 2, 2017
Phase: Phase 1
Study type: Interventional

This study is designed to identify a titration regimen of ABX-1431 in adults with neuropathic pain with satisfactory tolerability to central nervous system (CNS) adverse events (AEs). During the course of this study, each participant will take a daily dose of ABX-1431 or a matching placebo for 28 days.

NCT ID: NCT03120962 Not yet recruiting - Herpes Zoster Clinical Trials

Effect of Early Use of Oxycodone During the Acute Phase of Herpes Zoster on Preventing Postherpetic Neuralgia

Start date: May 2017
Phase: N/A
Study type: Interventional

Postherpetic neuralgia (PHN) which persists more than 90 days after the resolution of the acute shingles episode is the most common complication of herpes zoster. The continued pain or paresthesia not only affects patient quality of life, but also causes physical disability, emotional distress and social isolation. Conventional treatments for PHN are only partially work in some patients or not work at all in others. Once PHN presences, it is often refractory to the treatment, therefore, it is important to prevent the occurrence of PHN. In the study, the investigators want to identift whether the additional use of oxycodone therapy to current standard treatment in acute herpes zoster patients will decrease the incidence of post-herpetic neuralgia.

NCT ID: NCT03094195 Terminated - Clinical trials for Post-herpetic Neuralgia

Dose Response Study of EMA401 in Patients With Post-herpetic Neuralgia (PHN)

EMPHENE
Start date: June 27, 2017
Phase: Phase 2
Study type: Interventional

This study was designed to characterize dose response, and evaluate safety and efficacy of three different doses of EMA401 compared to placebo in patients with post-herpetic neuralgia (PHN).

NCT ID: NCT02701374 Completed - Clinical trials for Post-Herpetic Neuralgia

Efficacy and Safety of TRK-700 in Patient With Post-Herpetic Neuralgia

Start date: March 2016
Phase: Phase 2
Study type: Interventional

In Post-Herpetic Neuralgia(PHN) patients: - To conduct an explorative investigation of the efficacy and safety of repeated oral doses of TRK-700 via a randomized double blind comparative study - To measure the plasma concentration of TRK-700 and its metabolites

NCT ID: NCT02633306 Completed - Facial Pain Clinical Trials

Transcranial Magnetic Stimulation for Facial Pain

Start date: August 1, 2016
Phase: N/A
Study type: Interventional

Complex oro-facial pain is a poorly diagnosed and poorly treated cause of significant suffering and disability. This study will explore the ability of fMRI to identify patients with complex oro-facial pain who respond to transcranial magnetic stimulation therapy. Specific Aims: 1. To establish baseline patterns of MRI in patients with chronic oro-facial pain without a definitive etiologic diagnosis. 2. To estimate the rate of treatment success of transcranial stimulation of the primary motor cortex (M1) in these patients. 3. To identify post-treatment MRI patterns that are associated with treatment success.

NCT ID: NCT02607280 Completed - Clinical trials for Diabetic Peripheral Neuropathic Pain

DS-5565 Phase III Study for Renal Impairment in Japanese Subjects

Start date: December 2015
Phase: Phase 3
Study type: Interventional

Investigate the safety and efficacy of DS-5565 in Japanese subjects with Diabetic Peripheral Neuropathic Pain (DPNP) with renal impairment or Post-Herpetic Neuralgia (PHN) with renal impairment.

NCT ID: NCT02318719 Completed - Clinical trials for Post-Herpetic Neuralgia

DS-5565 Phase III Study for Post-herpetic Neuralgia

Start date: January 2015
Phase: N/A
Study type: Interventional

Investigate the efficacy and safety of DS-5565 in subjects with Post-Herpetic Neuralgia (PHN) in comparison to placebo