- Trials with a EudraCT protocol (24)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (25)
		
	   		
	   		    
                    
                   	
                   	    24 result(s) found for: ADAM.
                    
                
			
   			
		
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	| EudraCT Number: 2005-001411-22 | Sponsor Protocol Number: ADAM SPECT 3792 | Start Date*: 2006-02-15 | 
| Sponsor Name:University School of Medicine Hannover (MHH), represented by the chairmanship | ||
| Full Title: Serotonin-Transporter Binding in Tourette-Syndrome and Obsessive-Compulsive Disorder before and during Treatment with SRI: a I-123-ADAM-SPECT-Study | ||
| Medical condition: Obsessive compulsive disorder | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-000870-51 | Sponsor Protocol Number: CMCS240281 | Start Date*: 2013-02-25 | 
| Sponsor Name:Unidad de Gestión Clínica de Endocrinología y Nutrición | ||
| Full Title: RANDOMIZED CLINICAL TRIAL TO ASSESS THE EFFICACY OF TESTOSTERONE UNDECANOATE, METFORMIN, OR THE COMBINATION OF BOTH, FOR THE TREATMENT OF ISOLATED HYPOGONADOTROPIC HYPOGONADISM AND ERECTILE DYSFUNC... | ||
| Medical condition: Isolated hypogonadotropic hypogonadism related to obesity | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004592-35 | Sponsor Protocol Number: 6836 | Start Date*: 2010-06-16 | 
| Sponsor Name:Barts Health NHS Trust | ||
| Full Title: A Randomised Stratified Multicentre Phase II Clinical Trial of Single-Agent ADI-PEG 20 (Pegylated Arginine Deiminase) in Patients with Malignant Pleural Mesothelioma. | ||
| Medical condition: Mesothelioma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004406-93 | Sponsor Protocol Number: PDD-PC-01 | Start Date*: 2007-05-29 | |||||||||||
| Sponsor Name:Klinikum der Universität München | |||||||||||||
| Full Title: Photodynamische Diagnostik mit 5-Aminolävulinsäure zur Beurteilung der intraoperativen Absetzungsränder im Rahmen der radikalen Prostatovesikulektomie bei Patienten mit einem Prostatakarzinom | |||||||||||||
| Medical condition: Patients with prostate carinoma who will undergo radical prostatectomy. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003982-21 | Sponsor Protocol Number: P080402 | Start Date*: 2010-06-10 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Etude des transporteurs de la dopamine et de la sérotonine en imagerie TEMP utilisant les radiopharmaceutiques 123I-FP-CIT (datscan) and 123 I-ADAM dans la sclérose latérale amyotrophique et dans u... | |||||||||||||
| Medical condition: Patients présentant une SLA et volontaires sains | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000842-23 | Sponsor Protocol Number: AdAM_2017 | Start Date*: 2018-02-19 | 
| Sponsor Name:Medical University Innsbruck | ||
| Full Title: Adjuvante Imiquimod Therapie zur Senkung der Rezidivrate nach operativer Therapie bei analen HPV-Läsionen | ||
| Medical condition: anal HPV-lesions | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001224-33 | Sponsor Protocol Number: COV-HCQ | Start Date*: 2020-03-25 | |||||||||||
| Sponsor Name:Universitätsklinikum Tübingen | |||||||||||||
| Full Title: Randomized controlled trial of hydroxychloroquine versus placebo for the treatment of adult patients with acute coronavirus disease 2019 – COVID-19 | |||||||||||||
| Medical condition: Acute coronavirus disease 2019 | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001849-39 | Sponsor Protocol Number: NETs-C19 | Start Date*: 2020-05-18 | 
| Sponsor Name:Region Skåne | ||
| Full Title: Aerosolized DNase I for the treatment of severe respiratory failure in COVID-19 - a phase 2, randomized controlled trial | ||
| Medical condition: SARS-coronavirus-2 infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-011881-27 | Sponsor Protocol Number: ADAM | Start Date*: Information not available in EudraCT | |||||||||||
| 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: 2020-002612-52 | Sponsor Protocol Number: LUCAS | Start Date*: 2021-02-19 | ||||||||||||||||
| Sponsor Name:Department of Endocrinology, Rigshospitalet | ||||||||||||||||||
| Full Title: A randomized, double-blinded, clinical, placebo-controlled trial on the effects of therapy with Letrozole and hUman Choriongonadotropin in male hypogonadism induced by illicit use of Anabolic andro... | ||||||||||||||||||
| Medical condition: Male hypogonadism related to illicit use of anabolic androgenic steroids | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults | Gender: Male | |||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-005179-10 | Sponsor Protocol Number: ISS16694 | Start Date*: 2015-07-27 | 
| Sponsor Name:Charalampos Vlachopoulos | ||
| Full Title: Effect of long-term testosterone replacement therapy on arterial stiffness and endothelial function in male patients with hypogonadism | ||
| Medical condition: Male patients with hypogonadism | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: GR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001512-26 | Sponsor Protocol Number: COMIHY | Start Date*: 2020-04-22 | |||||||||||
| Sponsor Name:Universitätsklinikum Tübingen | |||||||||||||
| Full Title: Hydroxychloroquine for the treatment of mild COVID-19 disease | |||||||||||||
| Medical condition: Acute coronavirus disease 2019 | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003559-39 | Sponsor Protocol Number: 2011PP02 | Start Date*: 2013-10-01 | |||||||||||
| Sponsor Name:The University of Dundee [...] | |||||||||||||
| Full Title: Allopurinol and cardiovascular outcomes in patients with ischaemic heart disease (ALL-HEART) | |||||||||||||
| Medical condition: Ischaemic Heart Disease (IHD), angina or myocardial infarction | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-004254-37 | Sponsor Protocol Number: 000400 | Start Date*: 2022-06-27 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled trial to assess the efficacy and safety of FE 999049 for treatment of men with idiopathic infertility | |||||||||||||
| Medical condition: Idiopathic male infertility (including oligoasthenozoospermia) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: SE (Trial now transitioned) DE (Trial now transitioned) ES (Trial now transitioned) DK (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004641-16 | Sponsor Protocol Number: RG_18-272 | Start Date*: 2020-02-14 | |||||||||||||||||||||||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||||||||||||||||||||||
| Full Title: Letrozole or Clomifene, with or without metformin, for ovulation induction in women with polycystic ovary syndrome: a 2x2 factorial design randomised trial (The LOCI trial) | |||||||||||||||||||||||||||||||||
| Medical condition: Ovulation induction for women suffering from polycystic ovary syndrome | |||||||||||||||||||||||||||||||||
| 
 | |||||||||||||||||||||||||||||||||
| Population Age: Under 18, Adults | Gender: Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2023-000156-38 | Sponsor Protocol Number: 20230123SE | Start Date*: 2023-05-04 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Semmelweis University, Department of Internal Medicine and Oncology | ||||||||||||||||||||||||||||||||||||||
| Full Title: Value-based health economic comparative study of subcutaneous and intravenous trastuzumab-pertuzumab for HER-2 positive metastatic breast cancer based on patient reported outcomes. | ||||||||||||||||||||||||||||||||||||||
| Medical condition: HER-2 positive advanced breast cancer, locally unresectable or metastatic breast cancer | ||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: HU (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-003579-16 | Sponsor Protocol Number: BIOMIN | Start Date*: 2021-04-07 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:BIOMIN, a. s. | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: Multicenter, randomized, 52-week trial to determine the efficacy, adherence, safety, and tolerability of natural calcium and vitamin D3 and vitamin K2 supplementation, respectively, in postmenopaus... | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Osteopenia | |||||||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: SK (Completed) CZ (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-004742-42 | Sponsor Protocol Number: IFCT-1802 | Start Date*: 2019-08-29 | ||||||||||||||||
| Sponsor Name:IFCT | ||||||||||||||||||
| Full Title: A phase II single-arm trial evaluating safety and efficacy of Durvalumab in ECOG Performance Status 2-3, treatment-naive, patients with stage IV Non-Small Cell Lung Cancer (NSCLC) and high PD-L1 t... | ||||||||||||||||||
| Medical condition: Patient with a non small cell lung cancer and a poor general status | ||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2005-004451-35 | Sponsor Protocol Number: MRTSH01505 | Start Date*: 2007-03-13 | |||||||||||
| Sponsor Name:Genzyme Europe BV | |||||||||||||
| Full Title: Study to Evaluate the Dose, Safety and Effectiveness of Modified-Release Recombinant Human Thyroid Stimulating Hormone (MRrhTSH) When Used in Conjunction with Radioiodine for the Treatment of Multi... | |||||||||||||
| Medical condition: Nodular goiter are clinically recognizable enlargements of the thyroid gland characterized by excessive growth and structural and or functional transformation of one or several areas within the nor... | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DK (Completed) FR (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004329-10 | Sponsor Protocol Number: UKM17_0018 | Start Date*: 2020-07-09 | |||||||||||
| Sponsor Name:Westfälische Wilhelms-Universität Münster c/o Universitätsklinikum Münster, Geschäftsbereich Recht u. Drittmittel | |||||||||||||
| Full Title: A Randomized, open-label, Phase 2 Study of Adjuvant Apalutamide or Standard of Care in Subjects with High-risk, Localized or Locally Advanced Prostate Cancer After Radical Prostatectomy | |||||||||||||
| Medical condition: High risk adenocarcinoma of the prostate after radical prostatectomy (RPE) | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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