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NCT00612105 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Bausch Health Americas.

Completed
Registry status
Phase 2
Development phase
187
Enrollment target

NCT00612105: Completed Phase 2 study, sponsored by Bausch Health Americas.

NCT00612105 is a Phase 2 study that has completed, run by Bausch Health Americas. The registered enrollment target is 187 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (41% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00612105, a Phase 2 study, has completed, sponsored by Bausch Health Americas.

COMPLETED
Registry status
Phase 2
Development phase
187 participants
Enrollment target

Study Summary

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

Primary Outcome

Change from Baseline (BL) was calculated as the value of the average diary pain score for the last 7 days of the MP minus the value of the average pain score at BL (post wash-out period, including the average of the last 7 available entries prior to/including the diary pain measurement on Titration Day 0). Based on their pain experienced during the previous 24 hours, participants assessed their pain every evening at bedtime in an electronic diary by choosing the appropriate number on an 11-point

Interventions

  • DRUG Placebo
  • DRUG Retigabine

Trial Details

FieldValue
Enrollment Target 187 participants
Start Date 2007-10
Est. Completion 2009-12
Phase Phase 2
Bausch Health Americas

168 total trials

What the finished NCT00612105 record still lists

NCT00612105 is an interventional study that assigns participants to a tested intervention. The registered 187 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (41% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00612105 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00612105 about?

NCT00612105 is a clinical study titled "Safety/Efficacy Study of Retigabine vs. Placebo in Post-Herpetic Neuralgia (PHN)". The purpose of the study is to evaluate the efficacy of retigabine vs. placebo in reducing pain associated with post-herpetic neuralgia.

What is the current status of trial NCT00612105?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 187 participants. The study started on 2007-10. Estimated completion is 2009-12.

What interventions are being tested in trial NCT00612105?

The interventions under investigation include: Placebo (DRUG), Retigabine (DRUG).

Who is sponsoring clinical trial NCT00612105?

This trial is sponsored by Bausch Health Americas, which has 168 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00612105's enrollment target sits among peer trials

187 357th of 2000 higher than 1,644 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00612105, the US trial registry maintained by the National Library of Medicine. NCT00612105 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.