- Trials with a EudraCT protocol (829)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
829 result(s) found for: clinical observation.
Displaying page 1 of 42.
EudraCT Number: 2017-000292-83 | Sponsor Protocol Number: Tallisur | Start Date*: 2017-08-30 |
Sponsor Name:Servier Deutschland GmbH | ||
Full Title: Prospective, Multicenter, Open-label Phase IV trial of Trifluridine/Tipiracil to Evaluate the Health-related Quality of Life in Patients with Metastatic Colorectal Cancer | ||
Medical condition: Histologically or cytologically confirmed UICC stage IV carcinoma of colon or rectum with metastasis (metastatic colorectal cancer) with need for treatment due to progression | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001578-71 | Sponsor Protocol Number: App2018 | Start Date*: 2018-07-30 |
Sponsor Name:Göteborgs Universitet | ||
Full Title: Optimized treatment for uncomplicated acute appendicitis - active observation with or without antibiotic treatment. A phase IV consecutive clinical treatment trial. | ||
Medical condition: Acute appendicitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-016648-38 | Sponsor Protocol Number: C10953/3074 | Start Date*: 2010-08-06 |
Sponsor Name:Cephalon, Inc. | ||
Full Title: A 6-Month, Open-Label, Flexible-Dosage (150 to 200 mg/day) Extension Study of the Safety and Efficacy of Armodafinil Treatment as Adjunctive Therapy in Adults With Major Depression Associated With ... | ||
Medical condition: Major Depression Associated With Bipolar I Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) BG (Prematurely Ended) ES (Completed) DE (Prematurely Ended) FI (Completed) SK (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-004952-30 | Sponsor Protocol Number: E2080-J081-304 | Start Date*: 2017-02-13 |
Sponsor Name:Eisai Co, Ltd. | ||
Full Title: A Placebo-Controlled, Double-Blind Comparative Study of E2080 in Lennox-Gastaut Syndrome Patients | ||
Medical condition: Lennox-Gastaut Syndrome (LSG) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2009-010273-20 | Sponsor Protocol Number: 18081 | Start Date*: 2012-11-28 | |||||||||||
Sponsor Name:European organisation for research and treatment of Cancer | |||||||||||||
Full Title: Adjuvant peginterferon alfa-2b for 2 years vs Observation in patients with an ulcerated primary cutaneous melanoma with T(2-4)bN0M0: a randomized phase III trial of the EORTC Melanoma Group. | |||||||||||||
Medical condition: Ulcerated primary cutaneous melanoma >1mm (T2b-4bN0M0) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) DE (Completed) FR (Completed) AT (Completed) IT (Completed) DK (Completed) ES (Completed) NL (Completed) PT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002732-70 | Sponsor Protocol Number: YV25718 | Start Date*: 2012-02-09 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A Phase IIIb Parallel Group, Open Label Study of Pegylated Interferon alfa-2a Monotherapy (PEG-IFN, Ro 25-8310) Compared to Untreated Control in Children with HBeAg Positive Chronic Hepatitis B in ... | |||||||||||||
Medical condition: Treatment of HBeAg positive chronic hepatitis B (CHB) in children. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) DE (Completed) PL (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005284-13 | Sponsor Protocol Number: ARTO | Start Date*: 2018-10-09 | |||||||||||
Sponsor Name:DIPARTIMENTO DI SCIENZE BIOMEDICHE SPERIMENTALI E CLINICHE, UNIVERSITà DI FIRENZE | |||||||||||||
Full Title: A 2 arm, phase II controlled randomized trial comparing efficacy and safety of abiraterone and abiraterone associated with Ablative Radiation Therapy in patients with Oligometastatic castration res... | |||||||||||||
Medical condition: Oligometastatic prostate cancer, castration resistant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004240-30 | Sponsor Protocol Number: AIT-MULTIVIR-01 | Start Date*: 2014-06-18 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Prospective, open-label, randomised, two-arm, controlled, multicentre clinical trial, phase I/IIa, for the evaluation of safety and efficacy of an adoptive immunotherapy with allogeneic CMV-/EBV-sp... | |||||||||||||
Medical condition: Immune deficiency after allogeneic stem cell transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002490-19 | Sponsor Protocol Number: UKER-FECD-RIPA-01 | Start Date*: 2017-12-07 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Prospective single-centre randomized observer-blind placebo-controlled parallel-group phase IIa clinical trial to investigate the safety and efficacy of ripasudil 0.4% eye drops after descemetorhex... | |||||||||||||
Medical condition: Moderate to advanced Fuchs endothalial corneal dystrophy (FECD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001708-31 | Sponsor Protocol Number: Protokol_PPB_ACL_21042017 | Start Date*: 2017-06-20 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: The effect of the popliteal plexus block on postoperative pain after reconstruction of the anterior cruciate ligament | |||||||||||||
Medical condition: Postoperative pain after reconstruction of the anterior cruciate ligament | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003239-31 | Sponsor Protocol Number: HOVIR_700 | Start Date*: 2014-03-14 |
Sponsor Name:HOV GmbH | ||
Full Title: A randomised, placebo-controlled, single-centre, double-blind study to evaluate the efficacy, safety and tolerability of topically applied piroxicam gel in patients with recurrent herpes labialis | ||
Medical condition: Recurrent Herpes labialis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Temporarily Halted) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002618-38 | Sponsor Protocol Number: 721 | Start Date*: 2020-06-25 | |||||||||||
Sponsor Name:ASSOCIAZIONE "LA NOSTRA FAMIGLIA" - SEZIONE SCIENTIFICA I.R.C.C.S. "E.MEDEA" | |||||||||||||
Full Title: Clinical trial - phase II - to test safety and efficay of Etravirine's treatment in Friedreich Ataxia's patients | |||||||||||||
Medical condition: Friedreich's ataxia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004489-24 | Sponsor Protocol Number: IG1405 | Start Date*: 2018-09-13 |
Sponsor Name:Instituto Grifols, S.A | ||
Full Title: A Prospective, Randomised, Active-Controlled, Single-blind, Parallel Group Clinical Trial to Evaluate the Safety and Efficacy of Fibrin Sealant Grifols (FS Grifols) as an Adjunct to Haemostasis dur... | ||
Medical condition: Treatment of haemorrage during surgery | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BG (Completed) HU (Completed) DE (Completed) FR (Completed) SE (Prematurely Ended) GB (GB - no longer in EU/EEA) RO (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2022-001176-34 | Sponsor Protocol Number: BHV3000-407 | Start Date*: 2023-02-20 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: BHV3000-407: A Phase 4, Randomized, Doubleblind, Placebo-controlled Study to Evaluate the Efficacy and Tolerability of Rimegepant for the Prevention of Migraine in Adults with a History of Inadequa... | |||||||||||||
Medical condition: migraine headaches with or without aura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) IT (Trial now transitioned) FI (Trial now transitioned) DK (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004480-48 | Sponsor Protocol Number: 20446 | Start Date*: 2021-12-14 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A prospective, lead-in study to collect bleeding episodes, Factor VIII (FVIII) infusions, and patient-reported outcomes in patients with hemophilia A | |||||||||||||
Medical condition: Hemophilia A | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003303-18 | Sponsor Protocol Number: rl.01.2013 | Start Date*: Information not available in EudraCT |
Sponsor Name:Gedeon Richter Polska Sp. z o. o. | ||
Full Title: Clinical phase IV study assessing the efficacy and safety of the medicinal product Groprinosin in treatment of recurrent airway inflammation in children with impaired cellular immunity and diagnose... | ||
Medical condition: Recurrent airway inflammation in children with impaired cellular immunity. | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: PL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002796-23 | Sponsor Protocol Number: RHINO-CZ-2015-01 | Start Date*: 2015-09-10 |
Sponsor Name:Laboratoire de la Mer | ||
Full Title: Multicenter, parallel, randomized, single-blind trial comparing the efficacy and tolerability of Rhinaction®, an osmotic decongestant nasal spray containing essential oils versus Olynth® 0.1%, a va... | ||
Medical condition: Acute rhinitis Adults aged ≥18years old suffering from acute rhinitis with symptoms present for up to 72h. The purpose of this study is to demonstrate the efficacy and compare safety and tolerab... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024540-15 | Sponsor Protocol Number: C38072/3085 | Start Date*: 2011-07-20 | |||||||||||
Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | |||||||||||||
Full Title: An Open-Label Extension Study to evaluate the Long-Term Safety and Efficacy of Reslizumab (3.0 mg/kg) as Treatment for Patients with Eosinophilic Asthma who completed a prior Cephalon-sponsored Stu... | |||||||||||||
Medical condition: Treatment for patients with eosinophilic asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) SE (Completed) CZ (Completed) GR (Completed) HU (Completed) NL (Completed) DK (Prematurely Ended) PL (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002888-10 | Sponsor Protocol Number: SYD985.003 | Start Date*: 2020-03-25 | |||||||||||
Sponsor Name:Byondis BV | |||||||||||||
Full Title: A single-arm phase II trial to evaluate the safety and efficacy of the antibody-drug conjugate SYD985 in patients with HER2-expressing recurrent, advanced or metastatic endometrial carcinoma who pr... | |||||||||||||
Medical condition: Recurrent, Advanced or Metastatic Endometrial Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004572-36 | Sponsor Protocol Number: C-100-12 Part II | Start Date*: 2005-09-28 |
Sponsor Name:Antigenics Inc | ||
Full Title: A Multi-Center, Randomized, Phase 3 Study of Adjuvant Oncophage versus Observation in Patients with High Risk of Recurrence after Surgical Treatment of Renal Cell Carcinoma | ||
Medical condition: Renal cell carcinoma stage unspecified | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) AT (Completed) | ||
Trial results: (No results available) |
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