Clinical Trials Directory

Trials / Completed

CompletedNCT04063735

Alleviating Effects Against Dry Eye by Oral Intake of Cordyceps Cicadae Mycelia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
97 (actual)
Sponsor
David Pei-Cheng Lin · Academic / Other
Sex
All
Age
20 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Cordyceps cicadae mycelia was tested for amelioration of dry eye symptoms through dietary supplementation. Its efficacy in relief of human dry eye status was assessed by randomized, double-blinded tests, including multiple assessments. The results were compared between the placebo group and the experimental group.

Detailed description

Former animal studies had shown that Cordyceps cicadae mycelia can effectively ameliorate UVB-induced dry eye symptoms. This study further investigated its efficacy in human dry eye status by randomized, double-blinded tests, including dry eye questionnaires, blood tests, salivary tests, tear volume test, intra-ocular pressure assessments, ocular surface photography, corneal fluorescein stain, tear film breakup time test, fundus photography, and cornea impression cytology. All tests were performed again after 3 months of dietary supplement of either samples or placebo. A total of 97 participants completed the trial. The data were analyzed by paired-t test and compared between the placebo and the experimental groups.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCordyceps Cicadae MyceliaCordyceps Cicadae Mycelia supplement for 3 months
DIETARY_SUPPLEMENTPlaceboPlacebo was given to participants.

Timeline

Start date
2016-12-01
Primary completion
2017-02-07
Completion
2017-11-30
First posted
2019-08-21
Last updated
2019-08-21

Source: ClinicalTrials.gov record NCT04063735. Inclusion in this directory is not an endorsement.