- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Intracameral injection.
Displaying page 1 of 1.
EudraCT Number: 2018-002339-23 | Sponsor Protocol Number: MydriasisbeiMydrane | Start Date*: 2019-10-24 |
Sponsor Name:Medical University Graz, Department of Ophtalmology | ||
Full Title: Prospective intraindividual comparison of the mydriasis of a standardized intracameral anaesthetics with the topical preoperative drop application in the uncomplicated cataract surgery | ||
Medical condition: patients who need a cataract surgery in both eyes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005576-33 | Sponsor Protocol Number: LT2380-PII-09/12 | Start Date*: 2013-09-03 |
Sponsor Name:Laboratoires Théa | ||
Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaïne, phenylephrine and tropicamide) to obtain mydriasis in patients with small pupils for cataract surgery by phacoe... | ||
Medical condition: The primary aim of this study is to evaluate mydriasis obtained with T2380 (Fixed combination of lidocaïne, phenylephrine and tropicamide) in patients with small pupils | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-014054-14 | Sponsor Protocol Number: SILC 201109v2 | Start Date*: 2010-05-28 | ||||||||||||||||
Sponsor Name:Guys' and St Thomas' NHS Foundation Trust, Joint Clinical Trials Office | ||||||||||||||||||
Full Title: Comparison of the Safety of Intracameral Levofloxacin to intracameral Cefuroxime for the prevention of endophthalmitis in cataract surgery (SILC) | ||||||||||||||||||
Medical condition: Cataracts and endophthalmitis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003279-28 | Sponsor Protocol Number: LT2380-PII-11/07 | Start Date*: 2008-07-24 | |||||||||||||||||||||
Sponsor Name:Laboratoires Théa | |||||||||||||||||||||||
Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaïne, phenylephrine and tropicamide) for anaesthesia and mydriasis in phacoemulsification cataract surgery | |||||||||||||||||||||||
Medical condition: The aim of the development was to develop a combination of active substances enabling to obtain at the same time a mydriasis and an anaesthesia during cataract surgery. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Ongoing) ES (Ongoing) BE (Completed) PT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000838-19 | Sponsor Protocol Number: N12OLG | Start Date*: 2012-06-26 | |||||||||||
Sponsor Name:NKI-AVL | |||||||||||||
Full Title: High-dose alkylating chemotherapy in oligo-metastatic breast cancer harboring homologous recombination deficiency | |||||||||||||
Medical condition: Oligo metastatic breast cancer harboring homologous recombination deficiency and/or the patient has a deleterious germline BRCA1 or BRCA2 mutation | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021188-34 | Sponsor Protocol Number: LT2380-PIII-05/10 | Start Date*: 2011-07-01 | |||||||||||||||||||||
Sponsor Name:Laboratoires Théa | |||||||||||||||||||||||
Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaine, phenylephrine and tropicamide) for mydriasis and anaesthesia in phacoemulsification cataract surgery | |||||||||||||||||||||||
Medical condition: The aim of this clinical study will be to develop a combination of active substances enabling to obtain at the same time a mydriasis and an anaesthesia during cataract surgery | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PT (Completed) DE (Completed) BE (Completed) AT (Completed) ES (Ongoing) SE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000863-15 | Sponsor Protocol Number: 6020 | Start Date*: 2015-10-12 |
Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
Full Title: RANDOMIZED CONTROLLED CLINICAL TRIAL EVALUATING METHOTREXATE + BIOLOGIC VERSUS METHOTREXATE, SALAZOPYRINE AND HYDROXYCHLOROQUINEIN PATIENTS WITH RHEUMATOID ARTHRITIS AND INSUFFICIENT RESPONSE TO ME... | ||
Medical condition: RHEUMATOID ARTHRITIS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004890-21 | Sponsor Protocol Number: NL72427.068.19 | Start Date*: 2021-01-18 |
Sponsor Name:Academic Hospital Maastricht (azM) | ||
Full Title: Effectiveness of Periocular drug Injection in CATaract surgery | ||
Medical condition: cystoid macular edema (CME) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) PT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003277-34 | Sponsor Protocol Number: T2380-PIV-017 | Start Date*: 2018-01-15 | ||||||||||||||||
Sponsor Name:Laboratoires Théa | ||||||||||||||||||
Full Title: Phase IV, open-label, randomized clinical trial to evaluate the effects of Fydrane® and standard topical mydriatics and anaesthetics protocol on ocular surface after cataract surgery. | ||||||||||||||||||
Medical condition: Cataracts | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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