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NCT Number: NCT06570941

Benefits of a Cannabidiolic Acid Topical Cream for the Treatment of Restless Leg Syndrome

The goal of this open label clinical trial is to reduce the effects of restless leg syndrome. The main it questions it aims to answer are:

1. Reduce or eliminate the symptoms of restless leg syndrome. 2. Improve the quality of life of participants with restless leg syndrome.

Participants will be asked to apply the topical cream to the affected area 30 to 45 minutes before bedtime for 14 consecutive days.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Synthonics

Sarasota, Florida, 34238, United States

About this study

Restless Leg Syndrome (RLS) is multifactorial disease state with many different potential pathophysiological mechanisms, which includes dysfunctions from the cerebral cortex and spinal cord to mechanosensitive channels at the musculoskeletal periphery.1 Most therapeutic agents' effectiveness focuses on the CNS (e.g., dopaminergic drugs) or Renshaw cells. To our knowledge, therapeutic agents that are focused on the periphery were not very effective.

This technology focuses on the peripheral musculoskeletal component of the disease and is directed at treatment modalities that correct the dysfunction of mechanosensitive channels. By combining what is known about cannabinoids activity at the transient receptor potential channel of ankyrin 1 (TRPA1)2 and the role TRPA1 plays in regulating the shape and rigidity of the surrounding membrane structure at the Piezo channels3, an effective therapy at the site of discomfort should emerge. Moreover, the lessening of membrane tension is imparted by molecules that readily penetrate the membrane4, which Chylobinoid, the topical active ingredient, is uniquely designed to do.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with at least 3 month-course of symptomatic restless leg syndrome
  • Must meet International Restless Legs Syndrome Study Group (IRLSSG) criteria of at least mild symptoms.
  • Age > 18 years, including both males and females
  • Patient provides informed consent

Exclusion criteria

  • Previous operative procedure for treatment of RLS;
  • Current use of TENS (transcutaneous electrical nerve stimulation or plasma exchange;
  • Allergy to Cannabidiol (CBD) Cannabidiolic acid (CBDa), or any other ingredient contained in the topical cream;
  • Pregnant participants (participants who have the potential for being pregnant will sign a waiver), or breast feeding;
  • History of recreational substance abuse, fibromyalgia, Chronic Regional Pain Syndrome (CRPS), psychiatric history including but not limited to schizoaffective disorder, bipolar disorder, chronic depression, and suicidal ideation;
  • Conditions affecting capacity and adherence to study regimen including but not limited to dementia/delirium, Alzheimer's, Down's syndrome;
  • A need for elective surgery involving preoperative or postoperative analgesics or anesthetics during the study period;
  • No recent cannabinoid use in the last 2 months, and no use during the study.

Treatment and study plan

Chylobinoid Topical Cream

Drug

The topical cream is applied to the effected area to reduce or eliminate the symptoms of restless leg syndrome

Other names: Cannabidiolic acid topical cream

Primary outcomes

  1. Change of Restless Leg Syndrome

    Time frame: 14 days

    Severity of restless leg syndrome will be measured using the international restless leg syndrome questionnaire. It is a 10 question scale that is scored from 0 to 5 with 4 representing the most severe symptoms and 0 representing the least.

Secondary outcomes

  1. Patient Quality of Life in response to treatment

    Time frame: 14 days

    Change measured by Patients' Global Impression of Change scale (PGIC). The scale is 3 to -2 with 3 being much improved and -2 being much worse.

Sponsors and collaborators

Lead sponsor

Synthonics Inc

Industry

Registry information

Official study title

A Pilot Study to Investigate the Benefits of a Cannabidiolic Acid Topical Cream for the Treatment of Restless Leg Syndrome

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Aug 26, 2024
Registry last updated
Aug 28, 2024

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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