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NCT00568555 · ClinicalTrials.gov registry record · NA

Effects of Low Dose Naltrexone in Fibromyalgia

A NA study, sponsored by Stanford University.

Completed
Registry status
NA
Development phase
53
Enrollment target

NCT00568555: Completed NA study, sponsored by Stanford University.

NCT00568555 is a NA study that has completed, run by Stanford University. The registered enrollment target is 53 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00568555, a NA study, has completed, sponsored by Stanford University.

COMPLETED
Registry status
NA
Development phase
53 participants
Enrollment target

Study Summary

Low Dose Naltrexone (LDN) has been reported anecdotally to reduce the symptoms of Fibromyalgia, a Chronic Multisystem Illness. The drug may work by regulating natural pain-reducing systems. In this study, we will administer both LDN and placebo to a small group of individuals with Fibromyalgia and Gulf War Syndrome, both Chronic Multisymptom Illnesses, to assess the drug's efficacy in treating the condition.

Primary Outcome

Visual Analogue Scale for pain, 0 to 100, where 0=no pain and 100=worst pain imaginable. Baseline pain calculated averaging daily pain scores over the 2 week baseline period. Placebo and LDN pain scores calculated by averaging daily pain scores during the final 3 days of each condition. Values were converted to percent change in pain: \[(baseline pain - end point pain)/baseline pain\] x 100.

Interventions

  • DRUG Low Dose Naltrexone
  • DRUG Placebo - sugar pill

Trial Details

FieldValue
Enrollment Target 53 participants
Start Date 2007-06
Est. Completion 2010-01
Phase NA
Stanford University

1,744 total trials

What the finished NCT00568555 record still lists

NCT00568555 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 53 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

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

NCT00568555 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00568555 about?

NCT00568555 is a clinical study titled "Effects of Low Dose Naltrexone in Fibromyalgia". Low Dose Naltrexone (LDN) has been reported anecdotally to reduce the symptoms of Fibromyalgia, a Chronic Multisystem Illness. The drug may work by regulating natural pain-reducing systems. In this study, we will administer both LDN and placebo to a small group of individuals with Fibromyalgia and G...

What is the current status of trial NCT00568555?

This trial is currently completed. It is a NA study. The enrollment target is 53 participants. The study started on 2007-06. Estimated completion is 2010-01.

What interventions are being tested in trial NCT00568555?

The interventions under investigation include: Low Dose Naltrexone (DRUG), Placebo - sugar pill (DRUG).

Who is sponsoring clinical trial NCT00568555?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00568555's enrollment target sits among peer trials

53 1271st of 2000 higher than 729 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT00568555, the US trial registry maintained by the National Library of Medicine. NCT00568555 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.