- Trials with a EudraCT protocol (65)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (70)
65 result(s) found for: Urology.
Displaying page 1 of 4.
| EudraCT Number: 2012-002211-25 | Sponsor Protocol Number: bot001 | Start Date*: 2013-04-08 |
| Sponsor Name:Oslo University Hospital, Dept of Urology | ||
| Full Title: Prevention of bladder dysfunction in acute spinal cord injury A double-blind, randomized, placebo-controlled study to explore the effect of early treatment with Onabotulinumtoxin A in patients ... | ||
| Medical condition: Bladder dysfunction after acute spinal cord injury | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002592-29 | Sponsor Protocol Number: MIR-2014 | Start Date*: 2015-04-17 |
| Sponsor Name:Fakultní nemocnice Ostrava | ||
| Full Title: A randomized, double blind, placebo controlled study to evaluate the efficacy and safety of mirabegron 50 mg versus placebo in patients with neurogenic detrusor overactivity | ||
| Medical condition: Spinal cord injury Multiple sclerosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-005441-34 | Sponsor Protocol Number: 02none | Start Date*: 2009-06-04 | |||||||||||
| Sponsor Name:Department of Anesthesia, University College Hospital Galway | |||||||||||||
| Full Title: Comparison of Transversus Abdominis Plane (TAP) block, Ilioinguinal Nerve Block and Surgical Infiltration for Orchidoplexy and Hydrocele Repair in Children. | |||||||||||||
| Medical condition: Comparison of Transversus Abdominis Plane (TAP) block, Ilioinguinal Nerve Block and Surgical Infiltration for Orchidoplexy and Hydrocele Repair in Children. | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-001786-18 | Sponsor Protocol Number: CZOL446GDE08 | Start Date*: 2005-03-22 | |||||||||||
| Sponsor Name:EAU EUROPEAN ASSOCIATION OF UROLOGY | |||||||||||||
| Full Title: Effectiveness of Zometa treatment for the prevention of bone metastases in high risk prostate cancer patients. A randomized, open-label, multicenter study of the European Association of Urology (EA... | |||||||||||||
| Medical condition: Prevention of bone metastasis in high risk prostate cancer patients. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000099-27 | Sponsor Protocol Number: HEAT01 | Start Date*: 2017-04-26 | |||||||||||
| Sponsor Name:The Department of Urology | |||||||||||||
| Full Title: Toxicity of first-line abiraterone versus enzalutamide in men with metastatic castration-resistant prostate cancer: A randomized clinical trial | |||||||||||||
| Medical condition: Metastisc castration resistant prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-004961-14 | Sponsor Protocol Number: UV2013/4 | Start Date*: 2014-06-11 | |||||||||||
| Sponsor Name:Kliniken Kärnan Urology Centre | |||||||||||||
| Full Title: Pilot study to investigate the mode of action (MoA) of Uro-Vaxom® on a molecular level in pre-menopausal women suffering from recurrent urinary tract infections (rUTI) | |||||||||||||
| Medical condition: Recurrent urinary tract infections (rUTI) | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-001184-28 | Sponsor Protocol Number: PeP-RALP | Start Date*: 2022-10-11 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: Perioperative Propranolol in Robotic Assisted Laparoscopic Prostatectomy - A Pilot Study A parallel-group, phase 2, double-blind, 2-arm study to assess the feasibility of conducting a formal large... | ||
| Medical condition: Prostate Cancer | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-005164-27 | Sponsor Protocol Number: 260981 | Start Date*: 2008-02-22 |
| Sponsor Name:research office urology VUmc | ||
| Full Title: Botulinum toxin A intravesical injections in the treatment of Bladder Pain Syndrome/ Interstitial Cystitis | ||
| Medical condition: Interstitial Cystitis (IC) is a syndrome characterized by bladder pain associated with urgency, frequency, nocturia, dysuria and sterile urine. The patho-physiology remains largely unclear. No univ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-006198-98 | Sponsor Protocol Number: 99976 | Start Date*: 2009-10-05 |
| Sponsor Name:Isala klinieken Zwolle | ||
| Full Title: Pain management in renal colic; The efficacy of continuous intravenous administration of tramadol versus butylscopolamine. A double blinded, randomized placebo controlled, prospective multicenter t... | ||
| Medical condition: Renal colic pain based on kidney or ureteric stones in patients of 18 years and older. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-020397-42 | Sponsor Protocol Number: UROL2008/5 | Start Date*: 2010-12-22 |
| Sponsor Name:VUmc Dept Urology | ||
| Full Title: The efficacy of an antigenic marker lesion for the therapeutic effect in patients with multiple, Ta/T1, G1/G2, non-muscle invasive bladder cancer (NMIBC) treated with TUR followed by IL-2 instillation | ||
| Medical condition: Multiple, Ta / T1, G1 / G2, non-muscle invasive bladder carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002820-20 | Sponsor Protocol Number: OZBS62.14078 | Start Date*: 2016-02-03 | ||||||||||||||||
| Sponsor Name:Erasmus MC Dept. Urology | ||||||||||||||||||
| Full Title: Are alpha blockers effective in the treatment of bladder elimination problems in female patients with Multiple Sclerosis? | ||||||||||||||||||
| Medical condition: Bladder dysfunction in Multiple Sclerosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-002553-29 | Sponsor Protocol Number: kk-2013 | Start Date*: 2013-08-22 | ||||||||||||||||||||||||||
| Sponsor Name:Jens Sønksen | ||||||||||||||||||||||||||||
| Full Title: Metabolic changes due to iatrogenic hypogonadism in patients with prostate cancer: orchiectomy vs. triptorelin | ||||||||||||||||||||||||||||
| Medical condition: Men with prostate cancer where lifelong castration is indicated | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2021-001486-21 | Sponsor Protocol Number: 276046 | Start Date*: 2021-11-26 | |||||||||||
| Sponsor Name:University of Helsinki/CLUE working Group | |||||||||||||
| Full Title: A Multicentre Randomised Control Trial Assessing the Efficacy of Antimicrobial Prophylaxis for Extracorporeal Shock Wave Lithotripsy on reducing Urinary Tract Infections | |||||||||||||
| Medical condition: Nephrolithiasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-005295-33 | Sponsor Protocol Number: S54913 | Start Date*: 2013-03-08 | |||||||||||
| Sponsor Name:UZ Leuven-Department of Urology | |||||||||||||
| Full Title: Monocentric, open-label, phase III study that compares the efficiency and tolerance between intravesical oxybutynin and oral fesoterodine in children (5-16y) with neurogenic detrusor overactivity. | |||||||||||||
| Medical condition: children with neurogenic detrusor overactivity | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003720-43 | Sponsor Protocol Number: NIK-08-2014 | Start Date*: 2014-12-17 |
| Sponsor Name:Fakultní nemocnice Ostrava | ||
| Full Title: "Prevention of nicotine abstinence in critically ill patients after major surgery" | ||
| Medical condition: Nicotin abstinence delirium | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002466-20 | Sponsor Protocol Number: 4087 | Start Date*: 2012-08-16 | |||||||||||
| Sponsor Name:Royal Liverpool And Broadgreen University Hospitals NHS Trust | |||||||||||||
| Full Title: An exploratory, randomised, 3-way crossover study to determine the effect of paracetamol on urinary cystine excretion in cystinuria | |||||||||||||
| Medical condition: Cystinuria | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004853-26 | Sponsor Protocol Number: T315/2018 | Start Date*: 2019-03-25 | ||||||||||||||||
| Sponsor Name:Turku University Hospital | ||||||||||||||||||
| Full Title: The effect of androgen deprivation therapy on the expression of prostate specific membrane antigen (PSMA) in treatment naive metastatic prostate cancer | ||||||||||||||||||
| Medical condition: Metastatic prostate cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: FI (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-005840-87 | Sponsor Protocol Number: SAKK0110 | Start Date*: 2013-10-10 |
| Sponsor Name:Swiss Group for Clinical Cancer Research SAKK | ||
| Full Title: Carboplatin chemotherapy and involved node radiotherapy in stage IIA/B seminoma | ||
| Medical condition: Patients with seminoma stage IIA/B, after orchidectomy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-008692-33 | Sponsor Protocol Number: 2008-242 | Start Date*: 2009-04-21 | ||||||||||||||||
| Sponsor Name:Department of Urology, Herlev Hospital | ||||||||||||||||||
| Full Title: Evaluation of cytotoxicity and genetic changes of high dose vitamin C infusions in castration resistant metastatic human prostate cancer. | ||||||||||||||||||
| Medical condition: The effect of high dose intravenous weekly vitamin c infusion in castration resistant human prostate cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-001602-24 | Sponsor Protocol Number: Th.B-1(2007):BTX(CP/CPPS) | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Department of Urology and Pediatric Urology - Justus-Liebig-University Giessen | |||||||||||||
| Full Title: Intraprostatic injection of Botulinumtoxin type A in patients with chronic prostatitis / chronic pelvic pain syndrome (CP/CPPS) | |||||||||||||
| Medical condition: chronic prostatitis / chronic pelvic pain syndrom | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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