Skip to content

The Role of Ribose in Patients Diagnosed With Fibromyalgia

The Role of D-RIbose in Patients Diagnosed With Fibromyalgia

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00566514
Enrollment
200
Registered
2007-12-03
Start date
2006-07-31
Completion date
2008-07-31
Last updated
2008-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fibromyalgia

Keywords

fibromyalgia, ribose, d-ribose, dextrose

Brief summary

The purose of this research study is to determine the potential benefit of D-ribose, a nutritional supplement (a sugar), versus a placebo (another sugar) in people with fibromyalgia.

Detailed description

Two hundred to three hundred subjects (equally distribued between placebo and D-ribose) between 18-78 years of age will comprise this study. The final numbers enrolled will depend upon obtaining approximately 100 subjects that can display a high degree of compliance to TID dosing with approximately equal balance between the active and placebo arms.

Interventions

DIETARY_SUPPLEMENTD-ribose

5 grams administered orally TID

OTHERdextrose

5 grams orally TID

Sponsors

Bioenergy Life Science, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 78 Years
Healthy volunteers
No

Inclusion criteria

* previous diagnosis of fibromomyalgia by a MD * Has been diagnosed with fibromyalgia and are over 18 years of age * Does live in the United States

Exclusion criteria

* does NOT have severe medication/chemical/supplement sensitivities * does NOT have insulin dependent diabetes or other severe illnesses (cancer, hepatitis, congestive heart failure) * does NOT have rheumatoid arthritis or gout * previous use of ribose

Design outcomes

Primary

MeasureTime frame
Significant reduction in symptoms of pain and fatigue3 weeks

Secondary

MeasureTime frame
Demonstrate an improvement in ones quality of life3 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026