Comparing the Use of Vitamin c (Ascorbic Acid) in Eye Burn in Subconjunctival Injection to Topical or Oral Treatment.
NCT00734695 · Status: WITHDRAWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2010-03-02
Summary
Eye burns may cause a severe permanent damage. One kind of treatment is the use of vitamin C (Ascorbic acid). This study will compare between subconjunctival topical and/or systemic route of administration and topical and/or systemic administration.
Conditions
- Burn
Interventions
- DIETARY_SUPPLEMENT
-
vitamin c
Subconjunctival daily or bid
- DIETARY_SUPPLEMENT
-
vitamin c
topical and systemic
- DIETARY_SUPPLEMENT
-
vitamin c
topical systemic
Sponsors & Collaborators
-
Rambam Health Care Campus
collaborator OTHER -
Soroka University Medical Center
collaborator OTHER -
The Baruch Padeh Medical Center, Poriya
lead OTHER_GOV
Principal Investigators
-
naftali modi, MD · Baruch Pade medical center
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-07-31
- Primary Completion
- 2009-11-30
- Completion
- 2010-02-28
Countries
- Israel
Study Locations
More Related Trials
-
Investigator Initiated Study to Assess the Efficacy of OC-01 (Varenicline) Nasal Spray on Signs and Symptoms of Dry Eye Disease Following Photorefractive Keratectomy (PRK)
NCT05045508 ·Status: UNKNOWN ·Phase: PHASE3
-
The Role of Vitamin D in Corneal Epithelial Barrier Function, Ocular Microbiome, Ocular Inflammation, and Visual Acuity of Children With Allergic Conjunctivitis
NCT05839938 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Nasal Spray Study in Sjogren's Dry Eye Disease
NCT05700422 ·Status: COMPLETED ·Phase: PHASE4
-
The Ocular Microbiome in Patients With Dry Eye Disease
NCT04656197 ·Status: COMPLETED
-
Povidone-iodine 2% Eye Drop Versus Artificial Tear Drop for Treatment of Adenoviral Keratoconjunctivitis
NCT04041856 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
IIT Assessing OC-01Nasal Spray on Symptoms of DED Following CXL
NCT05136924 ·Status: UNKNOWN ·Phase: PHASE2
-
BMS-986325 in Healthy Participants and Participants With Primary Sjögren's Syndrome
NCT04684654 ·Status: TERMINATED ·Phase: PHASE1
-
Study to Evaluate the Safety, Tolerability, and Efficacy of OTX-CSI in Subjects With Dry Eye Disease.
NCT04362670 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Novel Combined Therapy for Refractory Vernal Keratoconjunctivitis
NCT03464435 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of BUFY01 Versus SVS20 in the Treatment of Dry Eye Disease
NCT05865379 ·Status: RECRUITING ·Phase: NA
-
A Randomized Controlled Trial to Evaluate the Safety and Efficacy of an Oral Supplement in Supporting Vision and Eye Health
NCT07123584 ·Status: COMPLETED ·Phase: NA
-
Evaluation of the Stinging Potential of Products in Human Eyes
NCT02872194 ·Status: COMPLETED ·Phase: NA
-
Comparative Study of 0.5% Carboxymethylcellulose With 0.005% Stabilized Oxychlorocomplex (PURITE™) Versus 0.5% Carboxymethylcellulose in the Treatment of Dry Eye
NCT00386646 ·Status: COMPLETED ·Phase: PHASE4
-
A Clinical Trial of Povidone-Iodine for the Treatment of Bacterial Corneal Ulcers
NCT00386958 ·Status: COMPLETED ·Phase: PHASE2
-
Corneal Uptake of Riboflavin Eye Drops
NCT04062435 ·Status: COMPLETED ·Phase: NA
-
A Phase 1/2, RU-101 Ophthalmic Solution in Patients With Severe Dry Eye
NCT01843894 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Cyclosporine and Intense Pulsed Light for Dry Eye in Contact Lens Users
NCT06392438 ·Status: RECRUITING ·Phase: PHASE3
-
Does the Use of a Moisture Chamber Decrease the Incidence of Corneal Abrasions in Critically Ill Pediatric Patients?
NCT00129077 ·Status: COMPLETED ·Phase: NA
-
OC-01 (Varenicline) Nasal Spray and Dry Eye Signs and Symptoms in Daily Disposable Contact Lens Wearers
NCT05161208 ·Status: COMPLETED ·Phase: PHASE4
-
Evaluation of the Stinging Potential of Sunscreen Products in Human Eyes
NCT02869113 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy Study of SJP-0035 Ophthalmic Solution in Patients With Moderate to Severe Corneal Epithelial Disorders
NCT02104388 ·Status: COMPLETED ·Phase: PHASE2
-
Comparison of Efficacy, Safety and Anti-Inflammatory Effect Between Topical 0.05%Cyclosporine A Emulsion and REFRESH® in Patients With Moderate to Severe Dry Eyes
NCT00704275 ·Status: UNKNOWN ·Phase: PHASE4
-
Ocular Microbiome and Immune System in Dry Eyes
NCT04658238 ·Status: RECRUITING
-
Dry Eye Symptom Mitigation by Oral Intake of Probiotics
NCT05906381 ·Status: COMPLETED ·Phase: NA
-
Effect of Topical Botulinum Toxin Eyedrop on Palpebral Fissure
NCT06080438 ·Status: TERMINATED ·Phase: PHASE4