CLINICAL TRIALS PROFILE FOR ALCAINE
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All Clinical Trials for ALCAINE
| Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
|---|---|---|---|---|---|---|
| NCT02951351 ↗ | Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections | Completed | Research to Prevent Blindness | N/A | 2016-10-12 | The specific aims of this study are to compare patient experience with and without a proparacaine drop after povidone iodine. |
| NCT02951351 ↗ | Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections | Completed | VitreoRetinal Surgery, PA | N/A | 2016-10-12 | The specific aims of this study are to compare patient experience with and without a proparacaine drop after povidone iodine. |
| NCT02951351 ↗ | Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections | Completed | Mayo Clinic | N/A | 2016-10-12 | The specific aims of this study are to compare patient experience with and without a proparacaine drop after povidone iodine. |
| NCT02973581 ↗ | SPI-directed Analgesia for Vitreoretinal Surgeries | Completed | Silesian University of Medicine | N/A | 2016-02-01 | The aim of this randomized trial is to assess the efficacy of SPI-directed analgesia for vitreoretinal surgeries (VRS), presence of PONV and oculocardiac reflex (OCR) and compare Numerical Rating Scale (NRS) with Surgical Pleth Index (SPI) for monitoring pain perception postoperatively. Patients received general anaesthesia alone or combined with either preemptive analgesia using topical solution of 0,5% proxymetacaine or peribulbar block (0,5% bupivacaine with 2% lidokaine) or preemptive intravenous infusion of 1,0 g of metamizol or preemptive intravenous infusion of acetaminophen in a doseof 10-15mg/kg of body weight. |
| NCT02973581 ↗ | SPI-directed Analgesia for Vitreoretinal Surgeries | Completed | Medical University of Silesia | N/A | 2016-02-01 | The aim of this randomized trial is to assess the efficacy of SPI-directed analgesia for vitreoretinal surgeries (VRS), presence of PONV and oculocardiac reflex (OCR) and compare Numerical Rating Scale (NRS) with Surgical Pleth Index (SPI) for monitoring pain perception postoperatively. Patients received general anaesthesia alone or combined with either preemptive analgesia using topical solution of 0,5% proxymetacaine or peribulbar block (0,5% bupivacaine with 2% lidokaine) or preemptive intravenous infusion of 1,0 g of metamizol or preemptive intravenous infusion of acetaminophen in a doseof 10-15mg/kg of body weight. |
| NCT03949101 ↗ | Atropine for Children and Adolescent Myopia Progression Study | Unknown status | Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine | Phase 4 | 2019-05-08 | Investigators are going to conduct a randomized controlled trial that myopic children are randomly allocated into two groups: combined use of 1% atropine and 0.01% atropine (experimental group) and 0.01% atropine (control group) in order to explore a better way to control myopia progression and eliminate adverse effects at the same time, provide reliably evidence for clinical guideline of atropine use in children, and investigate the mechanism of atropine on eyes. |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
Clinical Trial Conditions for ALCAINE
Condition Name
Clinical Trial Locations for ALCAINE
Trials by Country
Clinical Trial Progress for ALCAINE
Clinical Trial Phase
Clinical Trial Sponsors for ALCAINE
Sponsor Name
| Sponsor Name for ALCAINE | |
| Sponsor | Trials |
| Medical University of Silesia | 1 |
| Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine | 1 |
| Shanghai Eye Disease Prevention and Treatment Center | 1 |
| [disabled in preview] | 3 |
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