Active, not recruitingPHASE2, PHASE3NCT05660447
A Multi-Center Study on the Use of Rho-Kinase Inhibitor to Reduce or Prevent PVR in RRD Eyes at High Risk for PVR
Studying Vitreoretinopathy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Wills Eye
- Principal Investigator
- Jason Hsu, MDWills Eye Physicians-Mid Atlantic Retina, Wills Eye Hospital
- Intervention
- Netarsudil 0.02% Ophthalmic Solution [RHOPRESSA](drug)
- Enrollment
- 80 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2025
Study locations (1)
- Wills Eye Physicians - Mid Atlantic Retina, Philadelphia, Pennsylvania, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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