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Study identifier: NCT06541574 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Prevention of ProliFerative Vitreoretinopathy with Intravitreal MethotreXate in Primary Retinal DEtachment Repair (FIXER) Trial

Condition: Proliferative Vitreoretinopathy · Rhegmatogenous Retinal Detachment  ·  Sponsor: Cincinnati Eye Institute, Southwest Ohio

PhasePhase 2
Planned participants860
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

I. Title Prevention of ProliFerative Vitreoretinopathy with Intravitreal MethotreXate in Primary Retinal DEtachment Repair (FIXER) Trial * Today's Date: September 18, 2023 II. Principal Investigator * Principal Investigator: Christopher D. Riemann, M.D. (Cincinnati Eye Institute) * Email: criemann@cvphealth.com, Phone: 513-708-1979 V. Research Summary Purpose: To evaluate methotrexate for the prevention of PVR after primary rhegmatogenous retinal detachment repair. Methods: Inclusion Criteria: • Any adult patient, age ≥18 years-old, undergoing primary rhegmatogenous retinal detachment surgery with pars plana vitrectomy at the Cincinnati Eye Institute in Blue Ash, Ohio who is able to give informed consent. Exclusion Criteria: * Age \<18 years old * Pregnant patients or patients of child bearing potential unwilling to utilize long term contraception for the 12-week period spanning vitrectomy surgery for retinal detachment repair up until the 3 month postoperative visit. * History of endophthalmitis, ruptured globe or significant trauma in the affected eye * Chronic retinal detachment (symptoms greater than or equal to six weeks) * Any previous previous retinal detachment repair with pars plana vitrectomy, or scleral buckling surgery. Patients having undergone previous pneumatic retinopexy will not be excluded. * Presence of Grade C PVR: full thickness retinal folds or subretinal bands * Patients with contraindications to methotrexate, including breastfeeding, pr…

This description comes directly from the study's public registry record.

Talk to the study team

Christopher Riemann, MD  ·  513-708-1979  ·  criemann@cvphealth.com

Always discuss trial participation with your own doctor first.

Locations (1)

Cincinnati Eye InstituteCincinnati, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06541574