Ocular Effects of Synthetic Cannabinoids

Eye Manifestations Clinical Trial

— Bonsai  

Official title:

Ocular Effects of Synthetic Cannabinoids: A Case-control Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06235346
• Other study ID #: 2015/56
• Status: Completed
• Start date: March 15, 2015
• Est. completion date: January 15, 2016

Study information

• Verified date: January 2024
• Source: Bezmialem Vakif University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The goal of this observational study is to evaluate the ocular effects of Bonzai (synthetic cannabinoids) with spectral-domain optical coherence tomography.

Researchers will compare eye findings in patients who have previously used Bonzai with a healthy control group to see if there are ocular effects.

Description:

MATERIAL AND METHODS Participants This study was designed as cross-sectional, observational, case-control study. Upon referral from the judiciary-supervised probation unit of Alcohol and Substance Research, Treatment and Training Centre (AMATEM) of the relevant tertiary psychiatry hospital between March 2015 and January 2016, 60 eyes of 60 consecutive male patients with past synthetic cannabinoids (SC) use and 30 eyes of age-matched 30 male healthy control subjects were enrolled in the study in 3 groups: a control group (n=30) included eyes of subjects with no history of use of any substance including tobacco, a seronegative SC group (n=30) included eyes of patients declaring no present use of any substance, as verified by three consecutive negative urine toxicology tests performed two weeks apart, and a seropositive SC group (n=30), including eyes of patients with positive urine toxicology tests proving present use of SC.

SCs and relevant metabolites in urine samples were screened with a direct ELISA kit (K2 Enzyme Immunoassay, Immunalysis Corp., Pomona, CA, USA). This kit was able to detect relevant metabolites, such as JWH-018, JWH-073, and AM-2201, with a cut-off level of 20 ng/mL and over for positive results. Exposures to classical cannabinoids, ecstasy, amphetamines, opioids, and ethylene glycol were also screened.

Regarding SC use, the patients were asked about the duration and the last time of use. In addition, the previous use of other substances was questioned in detail.

Ophthalmic Assessments All eyes underwent ophthalmic examinations, including autorefraction, best-corrected visual acuity (BCVA) testing, biomicroscopy, non-contact IOP measurement, and dilated fundus examination.

An experienced technician performed spectral-domain optical coherence tomography (SD-OCT) imaging of all eyes following pupil dilatation (1% tropicamide) and systolic/diastolic blood pressure measurements (SBP/DBP). All SD-OCT assessments were conducted between 14:00 and 16:00 to minimize the potential effect of diurnal variation. Only high-quality SD-OCT images with a signal strength index (SSI) greater than 50 were sent for analysis. The parafoveal retinal thickness (parafoveal RT) and central foveal thickness (CFT), CT, peripapillary RNFL thickness, and macular GCC thickness measurements were performed with an RTVue-100 OCT device (Optovue Inc., Fremont, US), which had a 5 µm axial image resolution with a speed of 27,000 A-scans per second.

We preferred the ONH map protocol for examining the RNFL parameters. This protocol creates a RNFL thickness map based on measurements around a circle 3.45 mm in diameter centred on the ONH. The protocol for the GCC scan was based on examining a square grid (7 × 7 mm) on the central macula after centring 1 mm temporal to the macula. The average, superior, and inferior values displayed by the device were studied for the mean GCC and mean RNFL parameters.

Segmental divisions were recorded with the MM5 protocol of the inbuilt software, characterized by a 5 × 5 mm2 grid of 11 horizontal and 11 vertical lines with 668 A-scans and a 3 × 3 mm2 inner grid of 6 horizontal and 6 vertical lines with 400 A-scans for the retinal thickness of a 1 mm diameter CFT. The CT was measured by cross-sectioning through the foveolar centre line, characterized by an 8 mm width, with 1024 A-scans captured on the chorioretinal mode (these settings enable enhanced depth imaging along with contrast and brightness tuning). The line was rotated horizontally and vertically so that manual measurements were taken first at the central foveola and then 750 µm apart in the nasal, temporal, superior, and inferior directions with the ruler function, using a line extending from the posterior edge of the retinal pigment epithelium to the choroidoscleral junction.

The choroidal structure was analysed using the method previously described by Agrawal et al., and all collected images were processed and analysed using the open-source and publicly available ImageJ software (version 1.50a, freely available at http://imagej.nih.gov/ij/; National Institutes of Health [NIH], Bethesda, MD). According to this method, the image was first binarized using the Niblack auto-local thresholding function. This provided a clear visualization of the choroidoscleral interface while also enabling the precise selection of a region of interest, such as the total subfoveal choroidal area (TA). A fovea-centred, 1500 μm wide, nasal-to-temporal subfoveal choroidal area was manually selected using the polygon selection tool. The dark pixels representing the luminal area (LA) were selected using the colour threshold tool, and the residual light pixels were considered the stromal area (SA). The subfoveal CVI was calculated as the ratio of the LA to the TA. Manual measurements (CT and CVI) were carried out by the same experienced investigator blinded to the groups. Each measurement was repeated twice, and the mean of the two measurements was used in the analysis.

Statistical analysis Statistical analysis was conducted with software (SPSS 22.0 Version, IBM Corporation, New York, USA). Descriptive statistics were stated as the mean, standard deviation (SD), or median (Med), the interquartile range (Q1-Q3), and the frequency and ratio (%) values, where appropriate. The distribution of normality was evaluated for each parameter with the Kolmogorov-Smirnov test. Parametric (for normal distribution) or non-parametric tests were applied as appropriate. A parametric analysis of variance (ANOVA) with a post hoc Tukey test or a non-parametric Kruskal-Wallis test with a post hoc Bonferroni-corrected Mann-Whitney U test was used to analyse the independent variables. The chi-square test was used to analyse the qualitative data. Correlations of choroidal thickness measurements with parameters relevant to SC use were studied using the Spearman test.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 90
• Est. completion date: January 15, 2016
• Est. primary completion date: September 15, 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Male patients with past synthetic cannabinoids use and

• 30 eyes of age-matched 30 male healthy control subjects

Exclusion Criteria:

1. present co-use of any substances other than synthetic cannabinoids

2. chronic ocular disease, such as uveitis or glaucoma

3. history of previous ocular surgery

4. systemic disease, such as diabetes mellitus or hypertension

5. systemic or topical drug use that may influence vascular tone, such as topical anti-glaucomatous and systemic anti-hypertensive medications

6. refraction in spherical equivalent (SE) ± 1 dioptre (D) out of range. -

Related Conditions & MeSH terms

• Eye Manifestations

Locations

Country	Name	City	State
Turkey	Bakirkoy Dr. Sadi Konuk Educational and Research Hospital	Istanbul

Sponsors (1)

Lead Sponsor	Collaborator
Bezmialem Vakif University

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Agrawal R, Salman M, Tan KA, Karampelas M, Sim DA, Keane PA, Pavesio C. Choroidal Vascularity Index (CVI)--A Novel Optical Coherence Tomography Parameter for Monitoring Patients with Panuveitis? PLoS One. 2016 Jan 11;11(1):e0146344. doi: 10.1371/journal.pone.0146344. eCollection 2016. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Intraocular pressure	Intraocular pressure measurement by non-contact air-puff tonometer. Intraocular pressure will be reported in mmHg	All assessments were conducted between 14:00 and 16:00 to minimize the potential effect of diurnal variation.
Primary	Central foveal thickness	All measurements were obtained with the built-in software of the SD-OCT device. Central foveal thickness will be reported in µm.	All assessments were conducted between 14:00 and 16:00 to minimize the potential effect of diurnal variation.
Primary	Peripapillary retinal nerve fibre layer thickness	All measurements were obtained with the built-in software of the SD-OCT device. Peripapillary retinal nerve fibre layer thickness will be reported in µm.	All assessments were conducted between 14:00 and 16:00 to minimize the potential effect of diurnal variation.
Primary	Macular ganglion cell complex thickness	All measurements were obtained with the built-in software of the SD-OCT device. Macular Ganglion cell complex thickness will be reported in µm.	All assessments were conducted between 14:00 and 16:00 to minimize the potential effect of diurnal variation.
Primary	Subfoveal and perifoveal choroidal thicknesses	Choroidal imaging carried out with Spectral domain optical coherence tomography by chorioretinal mode. All choroidal thicknesses were measured with the built-in caliper function. Subfoveal and perifoveal choroidal thicknesses will be reported in µm.	All SD-OCT assessments were conducted between 14:00 and 16:00 to minimize the potential effect of diurnal variation.
Primary	Choroidal vascularity index	All choroidal images were exported to ImageJ software and binarized with Niblack autolocal thresholding method. After binarization, dark pixels indicate luminal area, and white pixels indicate stromal area. "Luminal area/total area(stromal+luminal area) * 100" formula will be used for choroidal vascularity index (CVI) calculation. CVI will be reported in %	All assessments were conducted between 14:00 and 16:00 to minimize the potential effect of diurnal variation.