Clinical Trials Logo

Clinical Trial Summary

This study will investigate the effects of lowering intraocular pressure by oral intake of Cordyceps cicadae mycelia, to provide evidence-based data for high intraocular pressure relief.


Clinical Trial Description

Study purpose This study investigated the effeicacy of oral Cordyceps cicadae mycelia for the relief of high intraocular pressure. Subjects 1. The total recruitment of subjects is 60 people, aged between 20 to 75 years. 2. Subjects with intraocular pressure more than or equal to 21 mmHg are included, irrespective of whether on us of Taflotan (saflutan). Methods 1. Informed consents will be obtained from subjects first. The subjects with pre-test intraocular pressure over or equal 21 mm Hg are advised to orally take two capsules containing a total of 500 mg of Cordyceps cicadae mycelia. After 90 minutes, the subjects are evaluated for intraocular pressure. The pre-test and and post-intake intraocualr pressure and blood pressure data will be compared by paired t test for significant differences if any. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05304299
Study type Interventional
Source Chung Shan Medical University
Contact
Status Completed
Phase N/A
Start date March 10, 2020
Completion date December 31, 2021

See also
  Status Clinical Trial Phase
Completed NCT04065061 - Erinacine A-enriched Hericium Erinaceus Mycelia for Improvement of Recognition, Vision, and Functional MRI Alterations N/A
Completed NCT01971723 - Multi-ingredient Supplement for Strength and Power N/A
Completed NCT04199234 - A Study to Compare the Tolerability of Microencapsulated Iron Compared to a Conventional Iron Supplement in the Market N/A
Completed NCT03769012 - Ability of Beta-glucan Supplementation to Augment Immune Function N/A
Completed NCT04063735 - Alleviating Effects Against Dry Eye by Oral Intake of Cordyceps Cicadae Mycelia N/A