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NCT00353808 · ClinicalTrials.gov registry record · Phase 2

A Trial Assessing The Long Term Safety And Tolerability Of [S,S]-Reboxetine In Patients With Post-Shingles Pain.

A Phase 2 study, sponsored by Pfizer.

Terminated
Registry status
Phase 2
Development phase
112
Enrollment target

NCT00353808: Clinical Trial Phase 2 study, sponsored by Pfizer.

NCT00353808 is a Phase 2 study that was terminated before completion, run by Pfizer. The registered enrollment target is 112 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (16% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00353808, a Phase 2 study, was terminated before completion, sponsored by Pfizer.

TERMINATED
Registry status
Phase 2
Development phase
112 participants
Enrollment target

Study Summary

The purpose of this study is to assess the long-term safety and tolerability of \[S,S\]-Reboxetine in patients with chronic pain following shingles. This is the extension study of Protocol A6061026.

Interventions

  • DRUG [S,S]-Reboxetine

Trial Details

FieldValue
Enrollment Target 112 participants
Start Date 2006-07
Est. Completion 2007-10
Phase Phase 2
Pfizer

1,845 total trials

Why NCT00353808 stopped before completion

NCT00353808 is an interventional study that assigns participants to a tested intervention. The registered 112 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (16% lower).

The record links to 0 conditions, and to 1 intervention - of which [S,S]-Reboxetine is the first listed.

NCT00353808 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00353808 about?

NCT00353808 is a clinical study titled "A Trial Assessing The Long Term Safety And Tolerability Of [S,S]-Reboxetine In Patients With Post-Shingles Pain.". The purpose of this study is to assess the long-term safety and tolerability of \[S,S\]-Reboxetine in patients with chronic pain following shingles. This is the extension study of Protocol A6061026.

What is the current status of trial NCT00353808?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 112 participants. The study started on 2006-07. Estimated completion is 2007-10.

What interventions are being tested in trial NCT00353808?

The interventions under investigation include: [S,S]-Reboxetine (DRUG).

Who is sponsoring clinical trial NCT00353808?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00353808's enrollment target sits among peer trials

112 631st of 2000 higher than 1,369 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 NCT00353808, the US trial registry maintained by the National Library of Medicine. NCT00353808 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.