- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,380 result(s) found.
Displaying page 1,778 of 2,219.
| EudraCT Number: 2022-001005-43 | Sponsor Protocol Number: STP225 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Biocodex | ||
| Full Title: Etude de l’intérêt de l’association du stiripentol (Diacomit®) et de la carbamazépine dans le traitement des patients atteints d’épilepsies focales pharmacorésistantes. | ||
| Medical condition: L’association carbamazépine/stiripentol est utilisée dans la pratique quotidienne à l’hôpital Necker chez les enfants atteints d’épilepsies focales. Il est donc pertinent d’étudier l’impact de cett... | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004514-10 | Sponsor Protocol Number: 00173 | Start Date*: 2017-03-08 |
| Sponsor Name:Raimo Tuuminen | ||
| Full Title: Pre and post-operative corticosteroid and NSAID combination treatment in cataract surgery of diabetic patient | ||
| Medical condition: Cataract senilis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004515-12 | Sponsor Protocol Number: 00174 | Start Date*: 2017-03-31 |
| Sponsor Name:Raimo Tuuminen | ||
| Full Title: Comparison between peri- and post-operative anti-inflammatory medication in cataract surgery: a randomized clinical trial | ||
| Medical condition: Cataract senilis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-005313-79 | Sponsor Protocol Number: 00175 | Start Date*: 2017-01-05 |
| Sponsor Name:Raimo Tuuminen | ||
| Full Title: Non-steroidal anti-inflammatory medication in cataract surgery | ||
| Medical condition: Cataract senilis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004784-40 | Sponsor Protocol Number: 00176 | Start Date*: 2017-03-03 |
| Sponsor Name:Raimo Tuuminen | ||
| Full Title: Anti-inflammatory medication in cataract surgery of pseudoexfoliation eyes | ||
| Medical condition: Cataract senilis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-003162-82 | Sponsor Protocol Number: 00171 | Start Date*: 2015-10-21 |
| Sponsor Name:Raimo Tuuminen | ||
| Full Title: treat-and-extend regimen (TER) in patients with diabetic macular edema | ||
| Medical condition: Diabetic macular edema | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004464-31 | Sponsor Protocol Number: PREGABACATPAIN | Start Date*: 2006-10-03 | |||||||||||
| Sponsor Name:Eija Kalso | |||||||||||||
| Full Title: Ahdistuksen vaikutukset neuropaattisessa kivussa ja pregabaliinin ahdistusta moduloiva vaikutus funktionaalisella magneettikuvauksella (fMRI) tutkittuna | |||||||||||||
| Medical condition: neuropaattinen kipu ahdistuneisuus | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004349-34 | Sponsor Protocol Number: 202003 | Start Date*: 2020-06-17 |
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: Early mental response to hormonal treatment in transgender men | ||
| Medical condition: Transsexualism | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-001866-17 | Sponsor Protocol Number: AMAG-FER-IDA-303 | Start Date*: 2011-09-16 | ||||||||||||||||
| Sponsor Name:AMAG Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: A Phase III, Open-Label Extension Trial of the Safety and Efficacy of Ferumoxytol for the Episodic Treatment of Iron Deficiency Anemia | ||||||||||||||||||
| Medical condition: Iron deficiency anemia (IDA) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: LV (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-002955-40 | Sponsor Protocol Number: 69HCL20_0111 | Start Date*: 2020-08-12 | |||||||||||
| Sponsor Name:Hospices Civils de Lyon | |||||||||||||
| Full Title: Postoperative analgesic effect of orally administrated nefopam after a total knee arthroplasty: a randomized controlled trial | |||||||||||||
| Medical condition: Major patients who have a surgery in the orthopedic surgery department of the Croix Rousse hospital for a total knee replacement. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-001903-42 | Sponsor Protocol Number: IPH5201-201 | Start Date*: 2023-03-07 | |||||||||||||||||||||
| Sponsor Name:Innate Pharma SA | |||||||||||||||||||||||
| Full Title: A Phase II Multicenter, open label, non-randomized study of neoadjuvant and Adjuvant Treatment with IPH5201 and durvalumab in patients with resectable, early-Stage (II to IIIA) Non-Small Cell Lung ... | |||||||||||||||||||||||
| Medical condition: Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2014-005188-34 | Sponsor Protocol Number: GORTEC2014-03 | Start Date*: 2015-04-20 | |||||||||||
| Sponsor Name:GORTEC | |||||||||||||
| Full Title: Phase III trial of laryngeal preservation comparating Induction chemotherapy with cisplatin, 5-fluorouracil and docetaxel (TPF) followed by radiotherapy and concomitant administration of radiother... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000273-81 | Sponsor Protocol Number: UC-GIG-2203 | Start Date*: 2022-09-13 | |||||||||||||||||||||
| Sponsor Name:UNICANCER | |||||||||||||||||||||||
| Full Title: Randomised phase II study evaluating trifluridine/tipiracil plus oxaliplatin versus FOLFOX in patients with gastric, oesophagus or gastroesophageal junction adenocarcinoma locally advanced, recurre... | |||||||||||||||||||||||
| Medical condition: Patients with gastric, oesophagus or gastroesophageal junction adenocarcinoma locally advanced, recurrent or metastatic, ineligible for triplet chemotherapy. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2021-002300-12 | Sponsor Protocol Number: EPOS_ZKSJ0134 | Start Date*: 2021-12-20 | |||||||||||
| Sponsor Name:Friedrich Schiller University | |||||||||||||
| Full Title: Epirubicin for the Treatment of Sepsis & Septic Shock | |||||||||||||
| Medical condition: Patients with sepsis or septic shock, currently hospitalized at the Intensive Care Unit (ICU) or Intermediate Care (IMC) regardless where the sepsis was first diagnosed. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000260-14 | Sponsor Protocol Number: UC-0140/1901 | Start Date*: 2020-01-30 | ||||||||||||||||
| Sponsor Name:UNICANCER | ||||||||||||||||||
| Full Title: Open-label, randomized, multicenter, phase III study, comparing standard chemotherapy to standard combination of endocrine therapy with Abemaciclib as initial Metastatic treatment among patients wi... | ||||||||||||||||||
| Medical condition: Untreated metastatic Estrogen Receptor positive (ER+), Human Epidermal Growth Factor Receptor-2 negative (HER2-) breast cancer with visceral involvement. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-002260-31 | Sponsor Protocol Number: GINECO-OV243b | Start Date*: 2020-10-01 | |||||||||||||||||||||
| Sponsor Name:ARCAGY-GINECO | |||||||||||||||||||||||
| Full Title: Multicentric non-randomized phase II of pembrolizumab in combination with etoposide-cisplatin-based chemotherapy in first-line advanced small cell ovarian carcinoma of hypercalcemic type | |||||||||||||||||||||||
| Medical condition: Advanced small cell ovarian carcinoma of hypercalcemic type | |||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2010-023263-18 | Sponsor Protocol Number: A0081105 | Start Date*: 2013-06-12 | |||||||||||
| Sponsor Name:Pfizer Inc 235 East 42nd Street, New York, NY10017 US | |||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTI-CENTER TRIAL OF PREGABALIN AS ADJUNCTIVE THERAPY IN PEDIATRIC AND ADULT SUBJECTS WITH PRIMARY GENERALIZED TONIC-CLONIC SEIZURES | |||||||||||||
| Medical condition: Primary Generalised Tonic Clonic Seizures | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) GB (Completed) HU (Completed) LT (Completed) NL (Completed) SK (Completed) AT (Completed) BG (Completed) ES (Completed) PL (Completed) EE (Completed) GR (Completed) BE (Completed) HR (Completed) DK (Completed) PT (Not Authorised) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004548-12 | Sponsor Protocol Number: RPL-001-16 | Start Date*: 2017-08-30 | |||||||||||
| Sponsor Name:Replimune Inc. | |||||||||||||
| Full Title: An Open-Label, Multicenter, Phase 1/2 Study of RP1 as a Single Agent and in Combination with PD1 Blockade in Patients with Solid Tumors [IGNYTE] | |||||||||||||
| Medical condition: Advanced solid tumours | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001744-62 | Sponsor Protocol Number: 2018/2727 | Start Date*: 2018-11-28 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Gustave Roussy | ||||||||||||||||||||||||||||||||||||||
| Full Title: A multicenter, open label, phase II basket trial exploring the efficacy and safety of the combination of rucaparib (PARP inhibitor) and atezolizumab (anti-PD-L1 antibody) in patients with DNA repai... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: •Molecularly selected cohorts that harbor DNA repair deficiency: –Non-Small Cell Lung Cancer –Urothelial Bladder Cancer –Metastatic Castration Resistant Prostate Cancer –Others: any histology, exce... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-002889-41 | Sponsor Protocol Number: UC-BCG-2103 | Start Date*: 2022-04-29 | ||||||||||||||||
| Sponsor Name:UNICANCER | ||||||||||||||||||
| Full Title: LESS: Single-arm study to de-escalate adjuvant endocrine therapy duration in women with HR+ HER2- breast cancer at very low risk of metastasis | ||||||||||||||||||
| Medical condition: Post-menopausal women with localized luminal A breast cancer and considered at low risk of metastatic relapse | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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