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NCT01315210 · ClinicalTrials.gov registry record · Phase 2

D-Ribose for Fatigue in Subjects With Fibromyalgia

A Phase 2 study of Fibromyalgia, sponsored by RiboCor.

Completed
Registry status
Phase 2
Development phase
110
Enrollment target
9
Study locations

NCT01315210 is a Phase 2 study of Fibromyalgia that has completed, run by RiboCor. The registered enrollment target is 110 participants, below the 178-participant average among 76 other Fibromyalgia trials with a reported enrollment target (38% lower). The trial reports 9 study locations across 6 states.

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The verdict

NCT01315210, a Phase 2 study of Fibromyalgia, has completed, sponsored by RiboCor.

COMPLETED
Registry status
Phase 2
Development phase
110 participants
Enrollment target
9
Study locations

Study Summary

To evaluate the safety and to determine the efficacy of D-ribose for the amelioration of fatigue in subjects with fibromyalgia. This is a phase IIa, randomized, double-blind, placebo-controlled, multi-center, multiple dose study of D-ribose versus placebo administered at doses of 5 g three times a day (TID) over a 12-week period to subjects who are experiencing fatigue associated with a diagnosis of fibromyalgia.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Placebo Powder
  • DRUG D-Ribose Powder

Study Locations (9)

Florida

  • Avail Clinical Research - DeLand
  • Renstar Medical Research - Ocala

Maryland

  • Columbia Medical Practice - Columbia
  • The Center for Rheumatology and Bone Research - Wheaton

North Carolina

  • Peters Medical Research - High Point
  • Wake Research Associates, LLC - Raleigh

California

  • Superior Research, LLC - Sacramento

Kentucky

  • University of Kentucky - Lexington

Pennsylvania

  • Altoona Center for Clinical Research - Duncansville

Trial Details

FieldValue
Enrollment Target 110 participants
Start Date 2011-05
Est. Completion 2012-10
Phase Phase 2

Sponsor

RiboCor

1 total trials

What the Registry Record Tells You About NCT01315210

The ClinicalTrials.gov registry entry for NCT01315210 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 178-participant average among 76 other Fibromyalgia trials with a reported enrollment target (38% lower). The listed sponsor is RiboCor, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Fibromyalgia appearing as the primary indexed condition, and to 2 interventions - of which Placebo Powder is the first listed.

NCT01315210 reports 9 study locations spanning 6 distinct geographic areas - top geographies include Florida, Maryland, North Carolina.

Frequently Asked Questions

What is clinical trial NCT01315210 about?

NCT01315210 is a clinical study titled "D-Ribose for Fatigue in Subjects With Fibromyalgia". To evaluate the safety and to determine the efficacy of D-ribose for the amelioration of fatigue in subjects with fibromyalgia. This is a phase IIa, randomized, double-blind, placebo-controlled, multi-center, multiple dose study of D-ribose versus placebo administered at doses of 5 g three times a d...

What is the current status of trial NCT01315210?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 110 participants. The study started on 2011-05. Estimated completion is 2012-10.

What conditions does trial NCT01315210 study?

This clinical trial studies the following conditions: Fibromyalgia.

What interventions are being tested in trial NCT01315210?

The interventions under investigation include: Placebo Powder (DIETARY_SUPPLEMENT), D-Ribose Powder (DRUG).

Who is sponsoring clinical trial NCT01315210?

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

Where is trial NCT01315210 being conducted?

This trial has 9 study locations across California, Florida, Kentucky, Maryland, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.