- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: Endocrinologist.
Displaying page 1 of 2.
EudraCT Number: 2020-002140-22 | Sponsor Protocol Number: Vitality | Start Date*: 2020-11-02 | |||||||||||
Sponsor Name:Lars møller Pedersen | |||||||||||||
Full Title: Gonadal dysfunction in male long-term survivors of malignant lymphoma | |||||||||||||
Medical condition: Hypogonadism | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003652-35 | Sponsor Protocol Number: 300 | Start Date*: 2006-02-02 |
Sponsor Name:Barnsley Hospital NHS Foundation Trust | ||
Full Title: A randomised, double blind, placebo controlled study to assess the effect of testosterone treatment on arterial stiffness in patients with type 2 diabetes, peripheral vascular disease and hypogonad... | ||
Medical condition: Male Hypogonadism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003678-82 | Sponsor Protocol Number: CHDR0606 | Start Date*: 2007-07-10 | |||||||||||
Sponsor Name:Centre for Human Drug Research | |||||||||||||
Full Title: Pharmacokinetics and effects of oral clonidine in children with suspected Growth Hormone deficiency | |||||||||||||
Medical condition: Clonidine is studied in the paediatric population, more specific children with short stature. It is used as a diagnostic tool to establish Growth Hormone reserve in routine practice. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005344-30 | Sponsor Protocol Number: TETRA-pilot | Start Date*: 2022-06-29 |
Sponsor Name:Amsterdam UMC, location VUmc | ||
Full Title: TETRA-pilot: Testosterone in transgender women after vaginoplasty: a dose-finding and feasibility pilot study | ||
Medical condition: Low testosterone levels in transgender women who underwent a vaginoplasty. We will investigate the serum testosterone levels at different doses of testosteron gel and if there are side effects. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002991-40 | Sponsor Protocol Number: A6281269 | Start Date*: 2015-04-01 |
Sponsor Name:Pfizer Inc | ||
Full Title: Evolution of Growth Rate in Children Suffering From a Disease Associated With Growth Retardation and Treated by Genotonorm. A Pilot Study | ||
Medical condition: Growth Disorders, Growth Retardation | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2020-004903-15 | Sponsor Protocol Number: 2020-004903-15 | Start Date*: 2022-04-20 |
Sponsor Name:University of Alabama at Birmingham | ||
Full Title: Denosumab (DMAB) Discontinuation and Switching Study in Glucocorticoid-Induced Osteoporosis (GIOP): A Pilot Study | ||
Medical condition: Glucocorticoid-Induced Osteoporosis (GIOP) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001845-15 | Sponsor Protocol Number: TINCRBEL_study | Start Date*: 2018-07-13 |
Sponsor Name:Academic medical centre, department of internal medicine | ||
Full Title: EvaluaTion of Clinical and laboratory outcomes of Rivaroxaban in short Bowel syndrome patients dEpending on Long term parenteral nutrition: a prospective cohort study (TINCRBEL study) | ||
Medical condition: Chronic intestinal failuyre (IF) is caused by large surgical bowel resection, severe motility, or absorption diseorders. These patientds require partial or total parenteral nutrition (PN and TPN, r... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002371-18 | Sponsor Protocol Number: I8B-MC-ITSB | Start Date*: 2019-03-29 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Prospective, Randomized, Double-Blind Comparison of LY900014 to Humalog with an Open-Label Postprandial LY900014 Treatment Group in Children and Adolescents with Type 1 Diabetes PRONTO-PEDS | |||||||||||||
Medical condition: Diabetes Mellitus, Type 1 | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) CZ (Completed) DE (Completed) FR (Completed) GB (GB - no longer in EU/EEA) AT (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004876-37 | Sponsor Protocol Number: PL37-C03-2013 | Start Date*: 2014-03-31 | |||||||||||
Sponsor Name:Pharmaleads SA | |||||||||||||
Full Title: A 4 week phase 2a, multicentre, randomised, double-blind, placebo-controlled add-on study into safety, tolerability and efficacy of 200 mg t.i.d. of PL37 in patients with peripheral neuropathic pa... | |||||||||||||
Medical condition: Neuropathic pain develops as a result of damage to, or dysfunction of, the system that normally signals pain. It may arise from a heterogeneous group of disorders that affect the peripheral and cen... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002992-17 | Sponsor Protocol Number: A6281271 | Start Date*: 2015-05-14 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: EVOLUTION OF GROWTH RATE IN CHILDREN WITH GROWTH RETARDATION RELATED TO LONG-TERM GLUCOCORTICOSTEROID THERAPY AND TREATED BY GENOTONORM® | |||||||||||||
Medical condition: Growth retardation related to long-term glucocorticoid therapy | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004493-42 | Sponsor Protocol Number: L-CP07-167 | Start Date*: 2014-12-03 | |||||||||||
Sponsor Name:Abbvie previously known as Abbott | |||||||||||||
Full Title: A Phase 3, Randomized, Multi-Center, Open-Label Study to Evaluate the Efficacy and Safety of Leuprolide Acetate 11.25 and 30 mg Formulations in Children with Central Precocious Puberty | |||||||||||||
Medical condition: Central Precocious Puberty | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004494-16 | Sponsor Protocol Number: L-CP07-177 | Start Date*: 2014-12-03 | |||||||||||
Sponsor Name:Abbvie previously known as Abbott | |||||||||||||
Full Title: A 36 Month, Multi-Center, Open-Label Extension Study to Evaluate the Safety of Leuprolide Acetate 11.25 mg and 30 mg Formulations in Children with Central Precocious Puberty | |||||||||||||
Medical condition: Central Precocious Puberty | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003963-31 | Sponsor Protocol Number: BEGAMI | Start Date*: 2007-11-19 | ||||||||||||||||
Sponsor Name:Karolinska Institutet | ||||||||||||||||||
Full Title: A three months, double-blind, randomized, parallell-group study evaluating the efficacy of sitagliptin (Januvia®) versus placebo on beta-cell function in patients with newly detected glucose abnorm... | ||||||||||||||||||
Medical condition: Patients with acute myocardial infarction or unstable angina pectoris and newly detected impaired glucose tolerance or type 2 diabetes (without any previous pharmacological glucose-lowering treatment) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001233-27 | Sponsor Protocol Number: PI2016_843_0008 | Start Date*: 2016-11-03 | |||||||||||
Sponsor Name:CHU Amiens Picardie | |||||||||||||
Full Title: Efficacity and safety of metformin extended release (XR) in diabetic patients with CKD in stages 1 to 3 (METXR/CKD) | |||||||||||||
Medical condition: type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013090-18 | Sponsor Protocol Number: NN2211-3619 | Start Date*: 2012-02-10 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 52-Week Randomised, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center, Multinational Exploratory Trial In Islet Cell Transplant Subjects With Type 1 Diabetes Mellitus To Evaluate The... | |||||||||||||
Medical condition: Diabetes Mellitus, Type 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001867-35 | Sponsor Protocol Number: NNCIT-02 | Start Date*: 2019-04-24 | |||||||||||
Sponsor Name:TikoMed AB | |||||||||||||
Full Title: Open, Randomized, Active Comparator-controlled, Multi-Center Study to Evaluate Safety and Efficacy of IBsolvMIR® in Islet Transplantation | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) NO (Ongoing) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004506-64 | Sponsor Protocol Number: 17000139BLC3002 | Start Date*: 2023-01-09 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 3, Open-Label, Multi-Center, Randomized Study Evaluating the Efficacy and Safety of TAR-200 in Combination with Cetrelimab or TAR-200 Alone Versus Intravesical Bacillus Calmette-Guérin (BCG... | |||||||||||||
Medical condition: BCG-naïve High-Risk Non-Muscle Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) PL (Trial now transitioned) IT (Ongoing) PT (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006794-37 | Sponsor Protocol Number: VRDN-001-101 | Start Date*: 2022-08-03 | |||||||||||
Sponsor Name:Viridian Therapeutics, Inc. | |||||||||||||
Full Title: A multiple ascending dose (MAD) safety, tolerability and efficacy study of VRDN-001, a humanized monoclonal antibody directed against the IGF-1 receptor, in normal healthy volunteers (NHVs) and sub... | |||||||||||||
Medical condition: Thyroid eye disease (TED) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) NL (Ongoing) IT (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002620-36 | Sponsor Protocol Number: 17000139BLC3001 | Start Date*: 2021-05-21 | ||||||||||||||||||||||||||
Sponsor Name:Janssen-Cilag International NV | ||||||||||||||||||||||||||||
Full Title: A Phase 3, Multi-center, Randomized Study Evaluating Efficacy of TAR-200 in Combination With Cetrelimab Versus Concurrent Chemoradiotherapy in Participants With Muscle-Invasive Urothelial Carcinoma... | ||||||||||||||||||||||||||||
Medical condition: Muscle-Invasive Urothelial Carcinoma (MIBC) of the Bladder | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) FR (Completed) PT (Ongoing) AT (Ongoing) PL (Completed) BE (Ongoing) HU (Ongoing) GR (Ongoing) CZ (Trial now transitioned) IT (Ongoing) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020437-12 | Sponsor Protocol Number: DT-DP-D2b | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:DermaTools Biotech GmbH | |||||||||||||
Full Title: A multicentric, double blind, randomized, comparative Phase II b study of the efficacy of a wound healing solution in patients with diabetic foot ulcer | |||||||||||||
Medical condition: diabetic foot ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) LV (Prematurely Ended) LT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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