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Completed

NCT Number: NCT00568035

Safety and Efficacy Study of QR-333 in Patient's With Symptomatic Diabetic Neuropathy

The purpose of this study is to determine whether QR-333 is safe and effective in the treatment of diabetic neuropathy as compared to placebo.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Parkway Medical Center, Birmingham, Alabama, United States

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About this study

Diabetic neuropathy is among the most common complication of diabetes, resulting in pain and numbness, which affects the patients sleep, functioning and well-being. The pain is often accompanied by unpleasant sensations described as buzzing, cramp-like, burning, or jolting. The pain is usually symmetrical and occurs in the upper and lower extremities following a "glove and stocking" distribution.

To date there is no fully effective treatment for diabetic neuropathy. Therapy is tailored individually according to subject complaints and may be selected from categories including Non-steroidal anti-inflammatory drugs (NSAIDs) and adjuvant analgesics (including tricyclic antidepressants and anticonvulsants).

The clinical trial is being conducted to determine the safety and efficacy of QR-333 in the treatment of diabetic neuropathy as compared to placebo.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diagnosis of diabetic neuropathy
  • must have some pain daily in the lower limbs due to diabetic polyneuropathy for at least 3 months prior to enrollment
  • must be willing to comply with study directions, write information in a diary (such as pain medications taken), read and comprehend written instructions, complete questionnaires, and have the ability to apply the cream as directed

Exclusion criteria

  • uncontrolled pain that has persisted for > 12 months.

Treatment and study plan

QR-333

Drug

QR-333 or placebo will be applied three times a day for 12 weeks

Primary outcomes

  1. Determine the safety of a three times daily application of QR-333 as compared to placebo.

    Time frame: 12 Weeks

Secondary outcomes

  1. Determine the efficacy of QR-333 on symptoms of diabetic neuropathy and the impact of QR-333 on the daily activities (including pain and sleep disturbance) of subjects with symptomatic diabetic neuropathy as compared to placebo.

    Time frame: 12 weeks

Sponsors and collaborators

Lead sponsor

Quigley Pharma, Inc.

Industry

Registry information

Official study title

Phase II Study of QR-333 for the Treatment of Symptomatic Diabetic Peripheral Neuropathy

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Dec 5, 2007
Registry last updated
Jan 8, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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