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NCT00857623 · ClinicalTrials.gov registry record · Phase 2

Study to Evaluate the Analgesic Efficacy of 28 Days' Oral Administration of AZD2066 Compared With Placebo in Patients With Painful Diabetic Neuropathy

A Phase 2 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 2
Development phase
127
Enrollment target

NCT00857623: Completed Phase 2 study, sponsored by AstraZeneca.

NCT00857623 is a Phase 2 study that has completed, run by AstraZeneca. The registered enrollment target is 127 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00857623, a Phase 2 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 2
Development phase
127 participants
Enrollment target

Study Summary

The purpose of this study is to investigate if AZD2066 can relieve the pain arising from painful diabetic neuropathy compared to placebo.

Primary Outcome

Change of mean pain intensity from 5-day baseline to the last 5 days of treatment, measured twice daily with NRS (12 hours recall). Mean pain intensity for 5-day baseline period (evening Day -6 to moning Day-1) and mean pain intensity for last 5 days on treatment (ie, last dose day and the 4 preceding calendar days) was calculated based on the numerical rating scale (NRS)(0-10). 0=No pain, 10=Worst pain imaginable.

Interventions

  • DRUG Placebo
  • DRUG AZD2066

Trial Details

FieldValue
Enrollment Target 127 participants
Start Date 2009-02
Est. Completion 2009-08
Phase Phase 2
AstraZeneca

1,285 total trials

What the finished NCT00857623 record still lists

NCT00857623 is an interventional study that assigns participants to a tested intervention. The registered 127 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

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

NCT00857623 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00857623 about?

NCT00857623 is a clinical study titled "Study to Evaluate the Analgesic Efficacy of 28 Days' Oral Administration of AZD2066 Compared With Placebo in Patients With Painful Diabetic Neuropathy". The purpose of this study is to investigate if AZD2066 can relieve the pain arising from painful diabetic neuropathy compared to placebo.

What is the current status of trial NCT00857623?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 127 participants. The study started on 2009-02. Estimated completion is 2009-08.

What interventions are being tested in trial NCT00857623?

The interventions under investigation include: Placebo (DRUG), AZD2066 (DRUG).

Who is sponsoring clinical trial NCT00857623?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00857623's enrollment target sits among peer trials

127 555th of 2000 higher than 1,445 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 NCT00857623, the US trial registry maintained by the National Library of Medicine. NCT00857623 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.