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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02080676
Other study ID # CMC-14-0001-CTIL
Secondary ID
Status Recruiting
Phase N/A
First received March 5, 2014
Last updated October 13, 2015
Start date March 2014
Est. completion date May 2016

Study information

Verified date October 2015
Source Carmel Medical Center
Contact Orna Geyer, MD
Phone 97248250926
Email orna_geyer@clalit.org.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Purpose of study: to check the effect of medical cannabis given for approved medical indications on ocular parameters including intra ocular pressure, optic nerve fibers thickness and choroidal thickness.


Description:

Purpose of study: to check the effect of medical cannabis given for approved medical indications on ocular parameters including intra ocular pressure, Retinal Nerve Fiber Layer (RNFL) thickness, optic nerve fibers thickness and choroidal thickness.

Adult patients with no ocular pathology that are being treated in the neurology or pain clinics with medical cannabis for different indications, were examined in the eye clinic.

First examination took place after the patient was not smoking for 5 hours. Three more examinations took place 1 hour 3 hours and 5 hours after smoking cannabis.

The following parameters were checked: blood pressure, pulse, visual acuity, intra ocular pressure, corneal thickness, axial length, slit lamp examination of anterior segment, fundoscopy and Optical Coherence Tomography (OCT) of the retina, and optic nerve.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date May 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Age over 18

- Treated with medical cannabis for approved medical indications

Exclusion Criteria:

- Known ocular pathology

- Topical or systemic treatment for intra ocular pressure

- Previous topical, intra ocular or systemic steroid treatment

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Carmel Medical Center Haifa

Sponsors (1)

Lead Sponsor Collaborator
Carmel Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intra ocular pressure 5 hours No
See also
  Status Clinical Trial Phase
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