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Neuralgia, Postherpetic clinical trials

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NCT ID: NCT04774458 Completed - Herpes Zoster Clinical Trials

Prospective Observation of the Fluoroscopy-guided Cervical Epidural Approach Using the Contralateral Oblique View

Start date: March 4, 2021
Phase: N/A
Study type: Interventional

The aim of the present study is to investigate the safety and clinical utility of contralateral oblique view for fluoroscopic guided cervical epidural access.

NCT ID: NCT04664530 Recruiting - Clinical trials for Postherpetic Neuralgia

The Study on the Esketamine in the Treatment of Postherpetic Neuralgia

Start date: November 25, 2020
Phase: Phase 4
Study type: Interventional

Herpes zoster (HZ) is an acute herpetic skin disease caused by the reactivation of the varicella-zoster virus (VZV) latent in the sensory ganglia. Postherpetic neuralgia (PHN) often occurs after herpes zoster heals and persists for a long time. At present, clinically anticonvulsants (such as gabapentin, pregabalin) and antidepressants (such as amitriptyline) are clinically first-line drugs for the treatment of PHN, which are not usually effective to treat PHN well, as well as to alleviate patients' bad mental symptoms. Esketamine, as a well-known N-methyl-D-aspartate receptor inhibitor, has both analgesic and antidepressant effects with extremely few incidence of respiratory depression, delirium, hallucinations, nausea and vomiting. Therefore, we hypothesize that esketamine could relieve PHN and Anxiety and depression-like symptoms symptoms in patients with PHN. This study intended to compare the efficacy of pregabalin, amitriptyline combined with esketamine therapy and pregabalin combined with amitriptyline therapy for alleviating PHN, and to further explore the feasibility and safety of esketamine in the treatment of PHN as well as underlying the mechanism of esketamine on the PHN.

NCT ID: NCT04662281 Completed - Clinical trials for Postherpetic Neuralgia

Efficacy and Safety of LX9211 in Participants With Postherpetic Neuralgia

RELIEF-PHN1
Start date: December 29, 2020
Phase: Phase 2
Study type: Interventional

Evaluation of the efficacy of LX9211 compared to placebo in reducing pain related to postherpetic neuralgia over an 11 week assessment period.

NCT ID: NCT04594226 Completed - Clinical trials for Postherpetic Neuralgia

Electroacupuncture Therapy for Treating Postherpetic Neuralgia

Start date: November 11, 2020
Phase: N/A
Study type: Interventional

Postherpetic neuralgia (PHN) has a high incidence rate and severely impact on quality of life and health care costs, interfering with physical, emotional and social functioning of affected patients. Current therapeutic options for PHN mainly include analgetic and local anaesthesia for selective nerve blockade. Nevertheless, the efficacy of analgetic is always limited by inevitable side effects, in which patients have poor compliance. Moreover, for some most suffering patients, the control of pain is often unsatisfactory despite the administration of complex combinations. As a non-pharmarceutical therapy, acupuncture is widely use for a wide range of pain conditions. Thus, it might be an alternative treatment for PHN. The aim of this multicenter randomized controlled trial is to investigate the efficacy and safety of electroacupuncture therapy in patients with postherpetic neuralgia.

NCT ID: NCT04560361 Recruiting - Clinical trials for Postherpetic Neuralgia

The Analgesic Effect of Electroacupuncture on Postherpetic Neuralgia

Start date: October 14, 2020
Phase: N/A
Study type: Interventional

The investigators designed the multicenter randomized parallel controlled clinical trial of electroacupuncture on PHN which is rigorously designed and have an appropriate sample size, aiming to evaluate the efficacy and safety of electroacupuncture in pain relieving and pain removing in the treatment of patients with PHN.

NCT ID: NCT04546334 Completed - Clinical trials for Postherpetic Neuralgia

Erector Spinae Plane Block in Post-herpetic Neuralgia

Start date: September 26, 2020
Phase: N/A
Study type: Interventional

This randomized clinical study will be carried out on 72 patients admitted to the pain clinic in Tanta University Hospitals with post-herpetic neuralgia. Cases presenting to the Pain Clinic with acute pain due to postherpetic neuralgia in thoracic and/or lumbar dermatomes with numerical rating scale (NRS) of 6 or more and they will be randomly divided, using the closed envelop method, into three equal groups. Group A (24 patients): Patients will be subjected to the routine medical treatment of post herpetic neuralgia as controls (Pregabalin, acyclovir, and paracetamol) and sham erector spinae plane block Group B (24 patients): Patients will be subjected to erector spinae block by bupivacaine (2 - 2.5 mg/kg, with a maximum of 175 mg/dose) together with medical treatment. Group C (24 patients): Patients that will subjected to erector spinae block by bupivacaine (2 - 2.5 mg/kg, with a maximum of 175 mg/dose with the addition of MgSO4 (equivalent to 100 mg)) together with medical treatment. Primary outcome will be the efficacy of pain relief Secondary outcome will be the frequency of pain and the consumption of analgesics.

NCT ID: NCT04530162 Withdrawn - Pain Clinical Trials

Prevention of Post Herpetic Neuralgia by Ultrasound Guided Single Nerve Block in the ED

Start date: October 1, 2021
Phase:
Study type: Observational

Herpes zoster causes significant morbidity on over 1 million Americans every year. Although the majority of herpes zoster pain will self-resolve within one week, a significant proportion of patients will develop postherpetic neuralgia (PHN), which is characterized by debilitating pain that persists more than three months after the initial symptoms. Nerve blocks have been previously studied as a method to control herpes zoster pain in outpatient pain clinics and inpatient settings. This study aims to investigate whether emergency department ultrasound guided nerve blocks can prevent PHN and effectively treat acute herpes zoster pain.

NCT ID: NCT04488835 Completed - Clinical trials for Neuralgia,Postherpetic

Pulsed Electromagnetic Field Therapy Versus Transcutaneous Electrical Nerve Stimulation in on Post-herpetic Neuralgia of the Sciatic Nerve

Start date: March 10, 2018
Phase: N/A
Study type: Interventional

Background and purpose: Post-herpetic neuralgia (PHN) is the most frequent chronic complication of herpes zoster, resulting in post- infectious severe neuropathic pain. Due to drug resistance severe pain; patients with PHN suffer from reduced physical activities, social and psychological manifestations as well as decrease in the quality of life. The purpose of this research was to evaluate the efficacy of pulsed electromagnetic field therapy (PEMFT) versus transcutaneous electrical nerve stimulation (TENS) in the treatment of post-herpetic neuralgia of the sciatic nerve. Methods: In an eight weeks period of treatemnt, 52 patients were randomly and equally assigned into two groups. Both groups received conventional physical therapy treatment protocol. Moreover, group (A) has an additional TENS application and group (B) had PEMFS application. TENS and the PEMFT were applied once daily, three times per week for 20 minutes for each session. Assessment performed pre and post intervention using visual analogue scale (VAS) and estimation of the carbamazepine intake (CMI).

NCT ID: NCT04467398 Recruiting - Clinical trials for Trigeminal Neuralgia

Incidence of Intravascular (IV) Injection During Trigeminal Nerve Blocks

Start date: July 20, 2020
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to investigate the incidence of intravascular injection during trigeminal nerve blocks.

NCT ID: NCT04313335 Completed - Clinical trials for Postherpetic Neuralgia

Duloxetine for PHN

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

In this study, the investigators aim to investigate the preventive efficacy of prophylactic oral duloxetine during acute herpes zoster on postherpetic neuralgia and its safety.