• Search
  • Helpdesk
  • Sales contact

Ophthalmology Clinical Trials

7 March 2024

Ophthalmic conditions and vision impairment currently affect 2.2 billion people globally:

  • Data collection can be very challenging for patients with visual impairment, but the patient- and site-centric research approach that we’ve seen growing for several years allows clinical trials to be better adapted to patient needs.
  • Measuring patients’ perception of their symptoms and their quality of life using efficient ePRO solutions is essential in ophthalmology clinical research.

Kayentis offers tailored decentralized solutions with qualitative ePROs and extensive experience in ophthalmology to ensure the success of ophthalmology clinical trials by:

  • securing ePRO data collection with adapted electronic devices and multiple data collection modes,
  • understanding and integrating patients’ specificities and preferences,
  • and anticipating unscheduled visits with strong product capabilities and processes

Download the case study 👇
Follow us on social media
Subscribe to our newsletter
About the author
Meet us at the following events

C-PATH 2025

APR 9-10 2025 • Rockville, Maryland, USA

OCT Europe 2025

APR 29-30 2025 • Barcelona, Spain
Booth #74 15th Annual Outsourcing in Clinical Trials Europe 2025 - Arena International

OCT East Coast 2025

MAY 20-21 2025 • King of Prussia, USA
Booth #44 16th Annual Outsourcing in Clinical Trials East Coast 2025 - Arena International

PCMG 2025

JUNE 10-12 2025 • Malaga, Spain
PCMG Annual Assembly 2025