- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Testicular pain.
Displaying page 1 of 1.
| EudraCT Number: 2020-004630-38 | Sponsor Protocol Number: HydroceleAlkScler | Start Date*: 2021-05-20 | ||||||||||||||||
| Sponsor Name:Region Jämtland/Härjedalen | ||||||||||||||||||
| Full Title: Sclerotherapy for hydro and spermatoceles with 99.5% Ethanol, an open clinical multicenter dose escalation study, phase 2 | ||||||||||||||||||
| Medical condition: Hydrocele and Spermatocele | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: SE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-002945-41 | Sponsor Protocol Number: 78464317 | Start Date*: 2020-09-24 | ||||||||||||||||||||||||||
| Sponsor Name:Lone Nikolajsen | ||||||||||||||||||||||||||||
| Full Title: The use of intraoperative methadone in children undergoing open urological surgery | ||||||||||||||||||||||||||||
| Medical condition: Postoperative pain in children undergoing open urological surgery | ||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | |||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2007-004609-85 | Sponsor Protocol Number: UV2005/01 | Start Date*: 2008-03-18 | ||||||||||||||||
| Sponsor Name:OM Pharma SA | ||||||||||||||||||
| Full Title: Multicentre, randomised, double-blind, placebo-controlled clinical study to assess the efficacy and safety of UroVaxom in chronic prostatitis and chronic pelvic pain syndrome (CP/CPPS) | ||||||||||||||||||
| Medical condition: Chronic prostatitis and chronic pelvic pain syndrome | ||||||||||||||||||
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| Population Age: Adults | Gender: Male | |||||||||||||||||
| Trial protocol: DE (Completed) AT (Completed) PT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-004729-42 | Sponsor Protocol Number: 22102014 | Start Date*: 2015-04-13 | |||||||||||
| Sponsor Name:Odense University Hospital, department M [...] | |||||||||||||
| Full Title: The effect of testosterone replacement in patients with hypogonadotroph hypogonadism due to opioid treatment for non-malignant disease A double-blinded, randomized and placebo-controlled trial | |||||||||||||
| Medical condition: Male Hypogonadism | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005938-15 | Sponsor Protocol Number: CloTASH-2021-2Version15.10.21 | Start Date*: 2021-11-03 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: Health risks and treatment of anabolic-androgenic steroid (AAS) induced hypogonadism among men – a pilot study exploring off-label use of clomiphene citrate to reduce symptoms of androgen deficienc... | ||
| Medical condition: Anabolic androgenic steroid induced hypogonadism among men | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-000406-35 | Sponsor Protocol Number: UX023-CL201 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Ultragenyx Pharmaceuticals Inc. | |||||||||||||
| Full Title: A Randomized, open Label, Dose Finding, Phase 2 Study to Assess the Pharmacodynamics and Safety of the anti-FGF23 antibody, KRN23, in Pediatric Patients with X-linked Hypophosphatemia (XLH) | |||||||||||||
| Medical condition: X-linked hypophosphatemia (XLH) is a disorder of renal phosphate wasting, and the most common heritable form of rickets. In XLH patients, high circulating levels of fibroblast growth factor 23 (FG... | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) NL (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-007969-23 | Sponsor Protocol Number: CC-5013-PC-002 | Start Date*: 2010-04-09 | |||||||||||
| Sponsor Name:Celgene Corporation | |||||||||||||
| Full Title: A PHASE 3 STUDY TO EVALUATE THE EFFICACY AND SAFETY OF DOCETAXEL AND PREDNISONE WITH OR WITHOUT LENALIDOMIDE IN SUBJECTS WITH CASTRATE-RESISTANT PROSTATE CANCER | |||||||||||||
| Medical condition: Chemo-naïve metastatic prostate cancer subjects with documented rising Prostate Specific Antigen (PSA) or documented Progressive Disease (PD) following hormonal therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: BE (Completed) HU (Completed) CZ (Prematurely Ended) DE (Completed) GB (Completed) AT (Completed) NL (Completed) IT (Completed) ES (Completed) DK (Completed) SE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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