- ICH GCP
- Registro de ensaios clínicos da UE
Últimos testes
EudraCT Number: 2009-013706-13 | Sponsor Protocol Number: TOP_LID_DPNP | Start Date: | ||||||
Sponsor Name: Wilhelminenspital der Stadt Wien | ||||||||
Full Title: ANALGESIC RESPONSE TO TRANSDERMAL LIDOCAINE IN PATIENTS WITH PAINFUL PERIPHERAL DIABETIC NEUROPATHY UNDERLYING DIFFERENT SENSORY PATTERNS | ||||||||
Medical condition: In this study the effect of transdermal lidocaine in patients with painful peripheral diabetic neuropathy will be examined. | ||||||||
|
||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: AT (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001519-39 | Sponsor Protocol Number: 2008-02-12-1 | Start Date: | ||||||
Sponsor Name: Biologiske Stasjon Drøbak | ||||||||
Full Title: Efficiency of a jellyfish sting inhibitor sun lotion and protocols for jellyfish sting pain relief | ||||||||
Medical condition: The degree of pain reduction in test subjects using a specific jellyfish (cnidaria) sting inhibitor and repellent lotion, compared to control subjects being protected by a normal water repellent su... | ||||||||
|
||||||||
Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: NO (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003621-10 | Sponsor Protocol Number: IC2011.05 | Start Date: | |||||||||||
Sponsor Name: INSTITUT CURIE | |||||||||||||
Full Title: CONSERVATIVE TREATMENT OF PATIENTS WITH RETINOBLASTOMA | |||||||||||||
Medical condition: RETINOBLASTOMA | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011881-27 | Sponsor Protocol Number: ADAM | Start Date: | |||||||||||
Sponsor Name: University Medical Center of the Johannes Gutenberg-University Mainz | |||||||||||||
Full Title: Changes of cerebral spinal fluid APPSα levels under oral therapy with acitretin 30 mg daily in patients with mild to moderate Alzheimer’s disease: a multicenter prospective randomised placebo-contr... | |||||||||||||
Medical condition: Alzheimer’s disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015642-35 | Sponsor Protocol Number: POVO-2009 | Start Date: | ||||||
Sponsor Name: medphano Arzneimittel GmbH | ||||||||
Full Title: Doppelblinde, randomisierte, kontrollierte, klinisch-experimentelle Studie der Phase II zum Nachweis der Wirksamkeit mittels Vasokonstriktionstest von Polcortolon® N Spray gegenüber Volonimat® Salb... | ||||||||
Medical condition: healthy volunteers. | ||||||||
|
||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: DE (Prematurely Ended) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001559-39 | Sponsor Protocol Number: 01/2005_01 | Start Date: | ||||||
Sponsor Name: Charité-Campus Mitte und Campus Virchow-Klinikum | ||||||||
Full Title: Randomisierte Phase II Studie zum Vergleich einer wöchentlichen Topotecangabe mit der Topotecangabe an fünf aufeinander folgenden Tagen bei Patientinnen mit platinresistentem rezidiviertem epitheli... | ||||||||
Medical condition: Patientinnen mit Ovarialkarzinom und Rezidiv / Progress | ||||||||
|
||||||||
Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2012-005226-29 | Sponsor Protocol Number: IBD-0337 | Start Date: | ||||||
Sponsor Name: Wolfson Medical Center | ||||||||
Full Title: Azithromycin Based Therapy for Induction of Remission in Active Pediatric Crohn's Disease | ||||||||
Medical condition: Crohn's disease | ||||||||
|
||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: NL (Ongoing) BE (Ongoing) PL (Completed) PT (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002787-68 | Sponsor Protocol Number: IMVT-1401-3201 | Start Date: | |||||||||||
Sponsor Name: Immunovant Sciences, GmbH | |||||||||||||
Full Title: A Phase 3, Multi-center, Randomized, Quadruple-masked, Placebo-controlled Study of Batoclimab for the Treatment of Participants with Active Thyroid Eye Disease (TED) | |||||||||||||
Medical condition: Thyroid Eye Disease (TED) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) IT (Ongoing) PL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004540-31 | Sponsor Protocol Number: Theophyllin_2 | Start Date: | ||||||
Sponsor Name: Universitätsklinikum Tübingen | ||||||||
Full Title: Monozentrische, randomisierte, placebo-kontrollierte Studie zur Evaluation der Nephroprotektion durch Theophyllin unter Cisplatin-haltiger Chemotherapie | ||||||||
Medical condition: evaluation of the nephroprotective efficacy of oral theophylline in patients treated with cisplatin | ||||||||
|
||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: DE (Prematurely Ended) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004058-11 | Sponsor Protocol Number: RM-493-023 | Start Date: | ||||||
Sponsor Name: Rhythm Pharmaceuticals, Inc. | ||||||||
Full Title: A Phase 3 trial of Setmelanotide (RM-493), a Melanocortin-4 Receptor (MC4R) Agonist, in Bardet-Biedl Syndrome (BBS) and Alström syndrome (AS) Patients with Moderate to Severe Obesity | ||||||||
Medical condition: Obesity and hyperphagia in patients with Bardet-Biedl Syndrome or Alström syndrome | ||||||||
|
||||||||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||
Trial protocol: FR (Completed) ES (Completed) GB (GB - no longer in EU/EEA) | ||||||||
Trial results: View results |