Retrospective Chart Review of Patients With Acanthamoeba Keratitis Who Have Received 0.8 mg/mL Polihexanide as Part of the "Medicines in Special Situations" (Medicamentos en Situaciones Especiales) Program in Spain.
NCT07195864 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 23
Last updated 2026-06-22
Summary
The study will be a multicentric, retrospective, non-interventional medical chart review of patients with AK who initiated a treatment with 0.8 mg/ml polihexanide as part of the Spanish Medicines in Special Situations program, whether they fully completed the treatment or not.
Baseline date is defined as the date of 0.8 mg/ml polihexanide initiation. The Study Period for each patient will be considered the period from the baseline to the conclusion of the treatment.
Conditions
- Acanthamoeba Keratitis
Interventions
- DRUG
-
PHMB 0.08%
The study population for this study is patients diagnosed with AK treated with 0.8 mg/ml polihexanide as part of the Spanish Medicines in Special Situations program.
Sponsors & Collaborators
-
SIFI SpA
lead INDUSTRY
Eligibility
- Min Age
- 12 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-10-30
- Primary Completion
- 2026-06-11
- Completion
- 2026-06-11
Countries
- Spain
Study Locations
More Related Trials
-
Evaluation of Dupilumab in Patients With Atopic Keratoconjunctivitis (AKC)
NCT04296864 ·Status: RECRUITING ·Phase: PHASE2
-
Phase III, Long-Term, Open-Label, Extension Study of 0.1% Tacrolimus(FK506) Ophthalmic Suspension in Patients With Vernal Keratoconjunctivitis
NCT00567918 ·Status: COMPLETED ·Phase: PHASE3
-
Exploratory Study of OPC-12759 Ophthalmic Suspension
NCT01493180 ·Status: COMPLETED ·Phase: PHASE2
-
Phase 2/3 Dose-Ranging Study of the Safety and Efficacy of OTX-101 in the Treatment of Keratoconjunctivitis Sicca
NCT02254265 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
EffiCacy, Safety and ToLErability of a Novel Ocular ANtiseptic for Ocular Use (CLEAN)
NCT05127525 ·Status: TERMINATED ·Phase: PHASE3
-
Safety, Efficacy, Tolerability and Pharmacokinetics of AGN-223575 Ophthalmic Suspension in Patients With Dry Eye Disease
NCT02435914 ·Status: COMPLETED ·Phase: PHASE2
-
Late Phase 2 Study of OPC-12759 Ophthalmic Suspension
NCT00475319 ·Status: COMPLETED ·Phase: PHASE2
-
Swiss PACK-CXL Multicenter Trial for the Treatment of Infectious Keratitis
NCT02717871 ·Status: COMPLETED ·Phase: PHASE3
-
The Antibiogram and Outcomes of Antimicrobial Regimens in Microbial Keratitis: A Prospective Cohort Study
NCT05655689 ·Status: COMPLETED
-
PK/PD, Safety and Tolerability of PHP-201 Topical Eye Drop in Korean and Japanese Healthy Subjects
NCT03586908 ·Status: COMPLETED ·Phase: PHASE1
-
Investigation of Preservative-Free Ophthalmic Solution in Ocular Dryness
NCT05778942 ·Status: COMPLETED
-
Phase 3 Study of OTX-101 in the Treatment of Keratoconjunctivitis Sicca
NCT02688556 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy Study of Rebamipide 2% Ophthalmic Suspension in Patients With Dry Eye
NCT01027013 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Tolerability of NTX-101 in Korean Healthy Volunteers
NCT05041543 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Efficacy Study of CF101 to Treat Keratoconjunctivitis Sicca
NCT00349466 ·Status: COMPLETED ·Phase: PHASE2
-
An Open-Label Extension of a Phase 3 Study of OTX-101 in the Treatment of Keratoconjunctivitis Sicca
NCT02845674 ·Status: COMPLETED ·Phase: PHASE3
-
Study Evaluating the Safety and Tolerability of NCX 4251 for the Treatment of Acute Exacerbations of Blepharitis
NCT03926026 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Safety and Efficacy of RVL-1201 in the Treatment of Blepharoptosis
NCT03565887 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Effectiveness of the PXL Platinum 330 System With Riboflavin Solution for Refractory Corneal Ulcers
NCT05255016 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
0.3% Sodium Hyaluronate Eye Drop to Prevent Recurrent Corneal Epithelium Exfoliation
NCT03000556 ·Status: UNKNOWN ·Phase: PHASE3
-
Study to Evaluate the Safety and Efficacy of CSB-001 Ophthalmic Solution 0.1% in Neurotrophic Keratitis Subjects
NCT04909450 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Pharmacokinetics, Safety, and Tolerability of rhEGF Eye Drops in Healthy Male Subjects
NCT05219461 ·Status: COMPLETED ·Phase: PHASE1
-
Pack Cross Linking for Infectious Keratitis
NCT05881187 ·Status: UNKNOWN ·Phase: NA
-
Evaluating the Safety, Tolerability, and Efficacy of GRF312 5% in Participants With Dry Eye Disease (DED).
NCT07264517 ·Status: COMPLETED ·Phase: PHASE2
-
Management of Eyelid Disorders by Ophthalmologists in Usual Medical Practice
NCT01552174 ·Status: COMPLETED