Exploring Enrollment and Engagement Trends in Individuals Managing Keratoconus: A Comprehensive Examination of Data on Keratoconus Clinical Trials
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Keratoconus
- Sponsor
- Power Life Sciences Inc.
- Enrollment
- 500
- Locations
- 1
- Primary Endpoint
- Number of keratoconus patients who remain in clinical trial until completion
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
This study aims to investigate the influences behind patient choices regarding involvement, discontinuation, or re-engagement in keratoconus clinical trials. Uncovering these factors is essential to enhance the relevance and efficacy of future research endeavors.
In essence, this trial aims to deepen understanding of the factors influencing participation in keratoconus clinical trials. Elevating participation rates could expedite the development of innovative treatments for this challenging condition.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Signed Written Informed Consent
- •Aged ≥ 18 years old
- •No prior treatment for keratoconus
Exclusion Criteria
- •Participant is actively receiving study therapy in another
- •Inability to provide written informed consent
- •Women of childbearing potential without a negative pregnancy test; or women who are lactating.
Outcomes
Primary Outcomes
Number of keratoconus patients who remain in clinical trial until completion
Time Frame: 12 months
Rate of patients who decide to join in a keratoconus clinical trial
Time Frame: 3 months