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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04423341
Other study ID # 1268646
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date May 20, 2020
Est. completion date October 1, 2021

Study information

Verified date October 2021
Source Silkiss Eye Surgery
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The planned study is a prospective analysis of non-psychoactive Cannabidiol (without THC) as an adjunctive therapy for blepharospasm in a masked double cross-over study. This prospective study is a follow-up to a retrospective study completed by the researchers using over-the-counter, self purchased CBD. This study will use FDA approved Cannabidiol medication, Epidiolex, directly from GW pharmaceuticals, rather than self-purchased CBD from the internet. Patients will undergo videorecording with a high resolution videocamera system at days 0, 45, 90, 135, and 180 using a novel blink analysis to gather objective data measurements of changes induced by CBD in Blepharospasm patients. This study will attempt to codify the data and quantify if adjunctive CBD therapy improves those areas compared to botulinum injection alone.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date October 1, 2021
Est. primary completion date March 22, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients in the private practice of the principal investigator with an ICD code of "blepharospasm" and: - undergoing routine maximal botulinum therapy - experiencing break through symptoms of spasm - marijuana naïve Exclusion Criteria: - concomitant diagnosis of epilepsy - patients whom are not marijuana naive - patients on concurrent anti-epileptics - patients who are pregnant or wishing to become pregnant - patients not wishing to participate in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Cannabidiol Oral Solution [Epidiolex]
100 mg BID for three months Placebo oral solution for three months

Locations

Country Name City State
United States Silkiss Eye Surgery Oakland California

Sponsors (4)

Lead Sponsor Collaborator
Silkiss Eye Surgery Benign Essential Blepharospasm Research Foundation, GW Pharmaceuticals Ltd., Smith-Kettlewell Eye Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Eyeblink analysis from high speed videocamera recordings - see separate outcome measures All patients will undergo video recording of their eyelid kinematics at days 0, 45, 90, 135, and 180. A high-resolution commercially available video camera will capture the eyelid positions at a sampling rate of thirty frames per second. Patients will be assessed in three different lighting conditions - in regular exam room lighting, under examination with the glare source of an indirect ophthalmoscope (at 2000 lux on both eyes from 5 feet), and in dim lighting. The upper and lower eyelid positions captured from each frame of the videos will be input into custom software developed by Visage Technologies, which fits a feature template to the facial features in each frame, including the upper and lower lids of each eye. The difference between the upper and lower lid positions defined the lid aperture, also known as the palpebral fissure. The eyeblink parameters will then calculated from the eyelid aperture time series with custom software written in MATLAB. 4 measurements over 6 months
Primary Median Blink Amplitude Measured in millimeters (mm) 4 measurements over 6 months
Secondary Median Blink Duration Measured in milliseconds (ms) 4 measurements over 6 months
Secondary Median Max Blink Velocity Measured in millimeters per milliseconds (mm/ms) 4 measurements over 6 months
Secondary Number of Blinks per 100ms Total "blinks" in 100 milliseconds (numeric value) 4 measurements over 6 months
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