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NCT Number: NCT06969417

Comparative Efficacy of Pregabalin and Lacosamide in Patients With Herpes Zoster and Post Herpetic Neuralgia

Post-herpetic neuralgia (PHN) is the most significant complication of herpes zoster caused by reactivation of latent Varicella-Zoster virus (VZV). PHN is characterized by neuropathic pain lasting beyond the resolution of the rashes. Post herpetic neuralgia (PHN) represents a potentially debilitating and often undertreated form of neuropathic pain that disproportionately affects vulnerable populations, including the elderly and the immunocompromised. PHN pain is typically localized, unilateral and chronic, but may be constant, intermittent, spontaneous and/or evoked. PHN is likely to interfere with sleep and daily activities.

Pregabalin is a gabapentinoid licenced for treatment of neurological disorders. It is one of the earlier drugs approved by the US Food and Drug Administration (2004) for the treatment of painful diabetic neuropathy and postherpetic neuralgia (PHN). Lacosamide (LCM) was approved in 2008 in the European Union and in the United States as adjunctive therapy for the treatment of focal-onset seizures with or without secondary generalization in adults and adolescents with epilepsy. Its efficacy has also been proven in neuropathic pain.

Although Pregabalin and Lacosamide have proven effective in various neuropathic pain disorder, comparative studies specifically for PHN remain scarce. This study aims to compare the efficacy of Pregabalin and Lacosamide in PHN patients, addressing the current gap in literature and providing clinically relevant insights to optimize treatment selection.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CMH Kharian Medical College

Kharan, Punjab Province, 50070, Pakistan

Location status: Recruiting

Location contact

Mushayada Irshad, MBBS, Mphil

CONTACT

[email protected]

+923237088421

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed cases of herpes zoster suffering from postherpetic neuralgia
  • Ages: 18 to 50
  • Both male and female

Exclusion criteria

  • Lack of consent
  • Patient already taking pain killers for post herpetic neuralgia
  • Patients suffering from other systemic illness

Treatment and study plan

Pregabalin

Drug

o Group A will receive Cap Pregabalin 150mg oral OD for 4 weeks

Lacosamide

Drug

o Group B will receive Tab Lacosamide 100mg oral BD for 4 weeks

Primary outcomes

  1. Visual Analog Scale

    Time frame: 4 weeks

    Pain intensity will be measured before and after treatment with help of Visual Analog Scale.

Study contacts

Contact information is provided by the study sponsor or research team.

Muhammad Waseem Shahid, MBBS, FCPS Dermatology

CONTACT

[email protected]

+923347202392

Mushayada Irshad, MBBS, MPhil Pharmacology

CONTACT

[email protected]

+92537532239

Sponsors and collaborators

Lead sponsor

CMH Kharian Medical College

Other Gov

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
May 13, 2025
Registry last updated
May 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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