Clinical Trials Logo

Peripheral Nerve Injuries clinical trials

View clinical trials related to Peripheral Nerve Injuries.

Filter by:

NCT ID: NCT02437695 Completed - Clinical trials for Peripheral Nerve Injuries

Robot Assisted Radical Prostatecomy and Positional Injury

Start date: May 2015
Phase: N/A
Study type: Observational

Although a condition for surgery, robotic interventions applied with steep Trendelenburg-lithotomy (ST-L) position may cause positional injury and peripheral neuropathy if good position is not achieved on the operating table. This study will be a 7-year retrospective examination of postoperative positional injury (PPI) in patients undergoing robot-assisted radical prostatectomy (RARP) for prostate diagnosis.

NCT ID: NCT02228928 Completed - Clinical trials for Postherpetic Neuralgia

Study of Capsaicin Patch for the Management of Peripheral Neuropathic Pain

Start date: February 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The efficacy and safety of the low concentration [0.65% (50 µg/cm2) and 1.25% (100 µg/cm2)] capsaicin patches and compared them to conventional 0.075% capsaicin cream and placebo patch in patients suffering from peripheral neuropathy

NCT ID: NCT02070367 Completed - Clinical trials for Peripheral Nerve Injuries

Somatosensory Assessment and Rehabilitation of Allodynia (SARA)

SARA
Start date: October 2014
Phase: N/A
Study type: Interventional

This pilot study will test a new therapy, somatosensory rehabilitation, for the painful sensitivity experienced by persons with nerve injuries and/or complex regional pain syndrome (CRPS). Several methods for measuring pain and sensitivity that emphasize the person's evaluation of their own symptoms and the impact of these symptoms on their daily activities will also be tested to make sure they are consistent and accurate. Previous research has suggested one of the assessments may also be used to assist in the identification of CRPS: this simple test will be evaluated to see if it can accurately identify persons with this disorder (for which there is currently no diagnostic test). Together, this will improve treatment of CRPS through early, accurate diagnosis and the ability to measure important changes in this painful condition, and set up future studies for this new rehabilitation treatment method.

NCT ID: NCT01954199 Completed - Low Back Pain Clinical Trials

The Effectiveness of Neurodynamic Techniques in Patients With Nerve-Related Leg Pain

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

This study aims to verify if patients with nerve-related leg pain benefits from neurodynamic treatment over two weeks.

NCT ID: NCT01713426 Completed - Clinical trials for Postherpetic Neuralgia (PHN)

A Study to Compare QUTENZA With Pregabalin for the Treatment of Peripheral Neuropathic Pain (PNP) After 8 Weeks of Treatment

ELEVATE
Start date: July 11, 2012
Phase: Phase 4
Study type: Interventional

This study is comparing the efficacy and tolerability of Qutenza with that of pregabalin in patients suffering from peripheral neuropathic pain. Treatment allocation will be to one of these treatments and the duration of the study will be about 10 weeks (assuming that from screening to treatment allocation takes 2 weeks). Participants will be asked to complete questionnaires about various aspects relating to their condition throughout the study. This study will include subjects suffering from Postherpetic Neuralgia, Peripheral Nerve Injury or Non Diabetic peripheral polyneuropathy.

NCT ID: NCT01596491 Completed - Clinical trials for Postherpetic Neuralgia

Study of Possible Changes in QST After Application of Capsaicin on Patients With Peripheral Neuropathic Pain

Start date: April 2011
Phase: N/A
Study type: Observational

The treatment of neuropathic pain ist still a challenge. A new promising therapy is the use of capsaicin on skin. The investigators first experiences with capsaicin in patients with peripheral nerve injury showed changes in the sensibility, which achieved its maximal extent after four weeks and was regressive, but not completely abolished 1,5 months after application. In this study the investigators hope to specify, how long and in which way exactly this changes in sensibility appear.

NCT ID: NCT01573650 Completed - Clinical trials for Peripheral Nerve Injury Digital Nerve Hand Left

Optimization of Peripheral Nerve Reconstruction: A Non-inferiority Trial

Start date: March 1, 2015
Phase:
Study type: Observational

1. To analyse the outcome of different treatment options of peripheral nerve repair with no gap (group 1) and with a critical sized (>5mm) defect (group 2) in order to optimize peripheral nerve repair 2. To reduce morbidity with the same outcome

NCT ID: NCT01416116 Completed - Clinical trials for Peripheral Neuropathic Pain (PNP) Due to Postherpetic Neuralgia (PHN)

Method of Pre-treatment for Application of QUTENZA Capsaicin 8% Patch

LIFT
Start date: July 6, 2011
Phase: Phase 4
Study type: Interventional

The Summary of product characteristics (SmPC) for QUTENZA advises that topical anaesthetic is applied prior to the application of QUTENZA. This is a multi-center, randomized, assessor-blinded study which will investigate the use of an oral analgesic as an alternative form of pre-treatment for QUTENZA.

NCT ID: NCT01302275 Completed - Clinical trials for Postherpetic Neuralgia

Oxcarbazepine for the Treatment of Chronic Peripheral Neuropathic Pain

IMIOXC
Start date: February 2011
Phase: Phase 4
Study type: Interventional

The purpose of this trial is to determine if the effect of oxcarbazepine on chronic peripheral nerve pain depends on the supposed mechanism of the pain, ie. if oxcarbazepine mainly relieve pain in patients with irritable nerves.

NCT ID: NCT01215760 Completed - Clinical trials for Median Nerve Disease

Sensory Reeducation in Peripheral Nerve Injuries of Hand

HandtherRCT
Start date: March 2009
Phase: N/A
Study type: Interventional

Objectives: To develop a protocol for early treatment using sensory reeducation through the mirror after surgical reconstruction of the median nerve and / or ulnar hand, and its comparison with the evolution of the return of skin sensitivity after a not early rehabilitation which will be conducted by physiotherapists, with blinding of the evaluators.