- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
25 result(s) found for: Prostaglandins.
Displaying page 1 of 2.
EudraCT Number: 2013-002484-26 | Sponsor Protocol Number: FIDEL | Start Date*: 2014-08-18 | |||||||||||
Sponsor Name:LFB Biomédicaments | |||||||||||||
Full Title: A RANDOMISED, MULTICENTRE, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY ON THE EFFICACY AND SAFETY OF A THERAPEUTIC STRATEGY OF POST PARTUM HAEMORRHAGE COMPARING EARLY ADMINISTRATION OF HUMAN FIBRINOGEN ... | |||||||||||||
Medical condition: post partum haemorrhage following vaginal delivery | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002965-20 | Sponsor Protocol Number: MISFOL2018 | Start Date*: 2019-05-14 | |||||||||||
Sponsor Name:SOLEDAD CARREGUI, NATIVIDAD BANEGAS, SARA CRUZ | |||||||||||||
Full Title: A randomized, open, 2 treatment arms clinical trial to evaluate the efficacy and safety of cervical ripening with Foley catheter vs cervical ripening with intravaginal synthetic analogue of prostag... | |||||||||||||
Medical condition: Cervical ripening prior labor induction | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019488-12 | Sponsor Protocol Number: Protocol No 1 | Start Date*: 2010-12-08 |
Sponsor Name:Joint Research Office, Barts and The London NHS Trust | ||
Full Title: A Single Centre Prospective Randomised Study to Investigate the Metabolism of Intravenous Paracetamol in Humans | ||
Medical condition: The study is looking at the cerebrospinal fluid pharmacokinetics of intravenous paracetamol. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000989-15 | Sponsor Protocol Number: DR200090 | Start Date*: 2021-07-28 | |||||||||||
Sponsor Name:University Hospital, Tours | |||||||||||||
Full Title: Oxytocin versus Prostaglandins for labor Induction of women with an unfavorable Cervix after 24 hours of cervical ripening: a multicenter non inferiority randomized trial | |||||||||||||
Medical condition: Labor Induction of women with an unfavorable Cervix after 24 hours of cervical ripening | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001914-27 | Sponsor Protocol Number: 13.0029 | Start Date*: 2017-08-24 |
Sponsor Name:St George's University Hospitals NHS Foundation Trust | ||
Full Title: Prostaglandin insert (Propess) versus tran-scervical balloon catheter for out-patient labour induction: A randomised controlled trial of feasibility (PROBIT-F) | ||
Medical condition: Induction of Labour | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004974-94 | Sponsor Protocol Number: 74460 | Start Date*: 2005-02-09 |
Sponsor Name:Santen Oy | ||
Full Title: Efficacy and safety of tafluprost 0.0015% eye drops as adjunctive therapy with timolol 0.5% eye drops. A randomised, placebo-controlled, phase III study in patients with open-angle glaucoma or ocul... | ||
Medical condition: Open angle glaucoma or ocular hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: EE (Completed) LV (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004982-28 | Sponsor Protocol Number: FFIS/PG/2017/03 | Start Date*: 2018-05-23 |
Sponsor Name:Fundación para la Formación e Investigación Sanitarias de la Región de Murcia | ||
Full Title: Phase IIb prospective, unicentric, randomized, parallel, double-blind, placebo-controlled clinical trial to evaluate the intravenous infusion of prostaglandins as therapy in patients with non-arter... | ||
Medical condition: Non-arteritic anterior ischemic optic neuropathy (NOIANA). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005609-34 | Sponsor Protocol Number: CNIO-BR-008 | Start Date*: 2016-04-26 | |||||||||||
Sponsor Name:Fundación CRIS de investigación para vencer el cáncer | |||||||||||||
Full Title: Abrogation of chronic monoclonal antibody treatment-induced T-cell exhaustion with DURVALUMAB (MEDI4736) in advanced HER-2 negative breast cancer: a pilot proof-of-concept trial | |||||||||||||
Medical condition: Advanced HER-2 negative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003692-12 | Sponsor Protocol Number: AZ02 | Start Date*: 2012-05-09 |
Sponsor Name:AZAD Pharma AG | ||
Full Title: A phase III , multicentre, randomised, investigator-masked, cross-over, comparative efficacy study of a generic Brinzolamide 10 mg/ml ophthalmic suspension (Azad Pharma AG) and Brinzolamide 10 mg/m... | ||
Medical condition: Patients suffering from open angle glaucoma and ocular hypertension with an elevated IOP, higher than 22mmHg and and lower or equal than 35 mmHg | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001738-33 | Sponsor Protocol Number: I14032 | Start Date*: 2015-09-24 | |||||||||||
Sponsor Name:CHU de LIMOGES | |||||||||||||
Full Title: Programmed Intermittent Epidural Bolus versus Continuous Epidural Infusion for third trimester voluntary termination of pregnancy analgesia : a randomized study. | |||||||||||||
Medical condition: Termination Pregancy | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005091-42 | Sponsor Protocol Number: 192024-041D | Start Date*: 2012-05-08 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: An Open Label (Stage 1) and Randomized (Stage 2), 24-Month Study of Safety and Efficacy of Bimatoprost Drug Delivery System in Patients With Open-Angle Glaucoma or Ocular Hypertension | |||||||||||||||||||||||
Medical condition: open-angle glaucoma (OAG) and ocular hypertension (OHT) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004529-99 | Sponsor Protocol Number: CanUTI-7 | Start Date*: 2015-11-17 | |||||||||||
Sponsor Name:Bionorica SE | |||||||||||||
Full Title: A double-blind, controlled, parallel-group, randomized, multicenter clinical trial to assess the efficacy and safety of a herbal drug containing centaury, lovage root, and rosemary leaf (CLR) in co... | |||||||||||||
Medical condition: Acute lower uncomplicated urinary tract infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000147-45 | Sponsor Protocol Number: YS001 | Start Date*: 2021-06-04 |
Sponsor Name:YONSUNG GMBH | ||
Full Title: A non-inferiority, randomized, investigator - masked, two-parallel group, phase III clinical trial, to evaluate the efficacy and safety of a preservative free formulation of latanoprost (YSLT) vers... | ||
Medical condition: GLAUCOMA, OCCULAR HYPERTENSION | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002383-27 | Sponsor Protocol Number: CHDR1806 | Start Date*: 2019-08-01 | |||||||||||
Sponsor Name:Centre for Human Drug Research | |||||||||||||
Full Title: An exploratory, single-center, double-blinded, healthy volunteer controlled study to characterize psoriasis patients and explore novel biomarkers for the treatment response of psoriasis with a mult... | |||||||||||||
Medical condition: Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2023-000142-42 | Sponsor Protocol Number: GR-2021-12373041 | Start Date*: 2023-04-17 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA | |||||||||||||
Full Title: Exploring the effect of a novel therapy on chronic intrathecal inflammation in patients with active progressive multiple sclerosis | |||||||||||||
Medical condition: patients with secondary progressive MS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001793-21 | Sponsor Protocol Number: CPA12001 | Start Date*: 2013-08-06 | |||||||||||
Sponsor Name:PHARMATHEN S.A. | |||||||||||||
Full Title: Efficacy and tolerability of brinzolamide in patients with elevated intraocular pressure: a double-blind, randomized, parallel, verum-controlled trial. | |||||||||||||
Medical condition: intraocular pressure increased | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003204-40 | Sponsor Protocol Number: PATHBP_2013 | Start Date*: 2014-01-20 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Paracetamol treatment in hypertension: effect on blood pressure | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Hypertension | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001727-39 | Sponsor Protocol Number: POP03 | Start Date*: 2018-10-16 | ||||||||||||||||
Sponsor Name:Polpharma S.A. | ||||||||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, INVESTIGATOR-MASKED, CROSSOVER, COMPARATIVE, NON-INFERIORITY TRIAL EVALUATING THE EFFICACY AND TOLERABILITY OF GENERIC LATANOPROST 0.05 MG/ML EYE DROPS SOLUTIO... | ||||||||||||||||||
Medical condition: Ocular hypertension and open angle glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-003387-27 | Sponsor Protocol Number: 848300145/0129/1POP04 | Start Date*: 2021-11-02 | ||||||||||||||||
Sponsor Name:Pharmaceutical Works Polpharma S.A. (Polpharma S. A.) | ||||||||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, INVESTIGATOR-MASKED, CROSS-OVER, COMPARATIVE, NON-INFERIORITY TRIAL OF GENERIC LATANOPROST + TIMOLOL (50μG + 5MG)/ML EYE DROPS, SOLUTION (POLPHARMA S.A.) COMPA... | ||||||||||||||||||
Medical condition: Ocular hypertension and open angle glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004307-14 | Sponsor Protocol Number: BECRO/ACT/LATANOS | Start Date*: 2021-02-12 | ||||||||||||||||
Sponsor Name:actrevo GmbH | ||||||||||||||||||
Full Title: Non-inferiority, Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a new Generic BAC-free Formulation of Latanoprost 0.05 mg/mL eye drops... | ||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension Elevated IOP and paediatric glaucoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Completed) | ||||||||||||||||||
Trial results: View results |
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