- Trials with a EudraCT protocol (165)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
165 result(s) found for: Prostatectomy.
Displaying page 1 of 9.
EudraCT Number: 2008-000588-41 | Sponsor Protocol Number: TRANEX-URO | Start Date*: 2008-02-26 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Tranexamic acid efficacy reducing surgery bleding in patients undergoing surgery for complete prostatectomy. | |||||||||||||
Medical condition: patients undergoing prostatic radical surgery for prostatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005246-31 | Sponsor Protocol Number: ANEST01 | Start Date*: 2017-03-20 |
Sponsor Name:Complexo Hospitalario Universitario de Pontevedra | ||
Full Title: Analgesic effectiveness of ultrasound-guided bilateral Transversus Abdominis Plane (TAP) block technique for laparoscopic radical prostatectomy: a prospective, randomized, simple-blind study | ||
Medical condition: Patients scheduled for elective laparoscopic radical prostatectomy surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022996-79 | Sponsor Protocol Number: URO 2010 | Start Date*: 2010-12-31 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: On demand versus daily sildenafil for patients undergoing bilateral nerve sparing radical prostatectomy: a randomized, open label, parallel group trial. | |||||||||||||
Medical condition: radical prostatectomy | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000674-30 | Sponsor Protocol Number: 2013-000674-30 | Start Date*: 2013-07-24 |
Sponsor Name:AOU SAN LUIGI GONZAGA - SCDU ONCOLOGIA MEDICA | ||
Full Title: Multicenter clinical trial, randomized phase II "window of opportunity" which aims to test the biological activity of abiraterone acetate administered as neoadjuvant therapy in patients with prosta... | ||
Medical condition: PROSTATE CANCER PATIENTS WITH HIGH RISK | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003523-16 | Sponsor Protocol Number: ARN-I-20-DEU-003-V01 | Start Date*: 2021-12-29 |
Sponsor Name:Universität des Saarlandes | ||
Full Title: A feasibility trial investigating inductive Apalutamide therapy combined with radical prostatectomy in patients with locally advanced T4 high risk prostate cancer | ||
Medical condition: patients with locally advanced T4 high risk prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005518-11 | Sponsor Protocol Number: 2006-10 | Start Date*: 2007-01-24 |
Sponsor Name:Örebro University Hospital | ||
Full Title: Epidural analgesia or opatient controlled regional analgesia for radical Retropubic Prostatectomy. A randomized, double-blind study. | ||
Medical condition: Postoperative pain after radical retropubic prostatectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003012-27 | Sponsor Protocol Number: 18062020 | Start Date*: 2021-01-12 |
Sponsor Name:Canisius Wilhelmina Ziekenhuis | ||
Full Title: Impact of peri-operative tEstosterone levels oN Functional and oncological Outcomes following RadiCal prostatEctomy | ||
Medical condition: Late-onset hypogonadism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002355-40 | Sponsor Protocol Number: SPCG 12 | Start Date*: 2005-08-23 |
Sponsor Name:Scandinavian prostate cancer group | ||
Full Title: An open randomized phase III trial of six cycles of docetaxel versus surveillance after radical prostatectomy in prostate cancer patients with high grade pT3 or margin positive pT2 | ||
Medical condition: Men, 18-70 years old, who have had radical prostatectomy due to prostate cancer and with a high grade pT3 or margin positive pT2 tumour may be candidates for the study. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Ongoing) FI (Completed) DK (Completed) IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004319-20 | Sponsor Protocol Number: 55218 | Start Date*: 2017-06-29 |
Sponsor Name:Maasstad Ziekenhuis | ||
Full Title: Spinal Morphine in Robotic Assisted Radical Prostatectomy | ||
Medical condition: Robotic Assisted Radical Prostatectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-014491-21 | Sponsor Protocol Number: | Start Date*: 2009-12-17 |
Sponsor Name:Cambridge University Hospitals NHS Trust | ||
Full Title: Neoadjuvant docetaxel prior to radical prostatectomy for high risk localised prostate cancer. Evaluation of biological and functional imaging surrogates of therapy efficacy. | ||
Medical condition: Neoadjuvant docetaxel prior to radical prostatectomy for high risk localised prostate cancer. Evaluation of biological and functional imaging surrogates of therapy efficacy | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-004562-35 | Sponsor Protocol Number: Ketolorac_001 | Start Date*: 2021-11-25 | ||||||||||||||||
Sponsor Name:Jessa ziekenhuis vzw | ||||||||||||||||||
Full Title: Low dose versus normal dose ketorolac for postoperative pain after prostatectomy and hysterectomy: a Double-blind Randomized Controlled Non-inferiority Trial | ||||||||||||||||||
Medical condition: Prostatectomy Hysterectomy | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004425-13 | Sponsor Protocol Number: PP01 | Start Date*: 2016-01-22 | |||||||||||
Sponsor Name:Skåne University Hospital, Department of Oncology | |||||||||||||
Full Title: Prospective evaluation of 68-Ga-PSMA-PET and early PSA kinetics during salvage radiotherapy for personalizing the management of men with relapse of prostate cancer after radical prostatectomy. | |||||||||||||
Medical condition: Patients with prostate cancer, with a PSA recurrence of ˃ 0.2 ng/ml after prostatectomy, and who are going to receive radiotherapy to the prostate bed. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011850-17 | Sponsor Protocol Number: H6D-EW-LVIK | Start Date*: 2009-10-23 | ||||||||||||||||
Sponsor Name:Eli Lilly and Company Limited | ||||||||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled Study to Evaluate the Effect on Unassisted Erectile Function of the Early Use of Tadalafil 5 mg Once a Day and Tadalafil 20 mg On Demand Treatment for... | ||||||||||||||||||
Medical condition: Erectile dysfunction following Bilateral Nerve-Sparing Radical Prostatectomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) FR (Completed) PL (Completed) BE (Completed) GB (Completed) IT (Completed) PT (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003599-39 | Sponsor Protocol Number: SAKK08/15 | Start Date*: 2017-12-13 |
Sponsor Name:Swiss Group for Clinical Cancer Research (SAKK) | ||
Full Title: PROMET - Multicenter, Randomized Phase II Trial of Salvage Radiotherapy +/- Metformin for Patients with Prostate Cancer after Prostatectomy | ||
Medical condition: Histologically confirmed adenocarcinoma of the prostate without small cell features with PSA progression after radical prostatectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DE (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-018311-15 | Sponsor Protocol Number: GE-148-003 | Start Date*: 2010-05-21 |
Sponsor Name:GE Healthcare Limited | ||
Full Title: A Phase 2, Open-label Study to Assess the Uptake and Retention and Safety of GE 148 (18F) Injection in Subjects with Biopsy-proven Prostate Cancer who are Scheduled for Radical Prostatectomy | ||
Medical condition: Detection of abnormal amino acid transport using Positron Emission Tomography (PET) in malignancy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Prematurely Ended) FI (Prematurely Ended) DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002485-31 | Sponsor Protocol Number: OPIP | Start Date*: 2017-01-31 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Optimisation of [68Ga] PSMA-11 PET/CT Imaging Protocol for localizing primary prostate cancer prior to radical prostatectomy | ||
Medical condition: Primary localised prostate cancer, in men who opt for active treatment in the form of a radical prostatectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004991-16 | Sponsor Protocol Number: tba | Start Date*: 2022-09-28 |
Sponsor Name: | ||
Full Title: 177Lu-PSMA RADIOLIGAND THERAPY IN PATIENTS WITH LYMPH NODE METASTATIC HORMONE-SENSITIVE PROSTATE CANCER UNDERGOING ROBOT-ASSISTED LAPAROSCOPIC RADICAL PROSTATECTOMY AND EXTENDED PELVIC LYMPH NODE D... | ||
Medical condition: prostate cancer, eligible for radical prostatectomy and extended pelvic lymph node dissection, with 1-3 pelvic nodal metastases on preoperative PSMA PET | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004585-18 | Sponsor Protocol Number: KKS-190 | Start Date*: 2013-08-27 | |||||||||||||||||||||
Sponsor Name:Philipps-Universität Marburg | |||||||||||||||||||||||
Full Title: Perioperative administration of Tapentadol – tolerance, safety and effects on postoperative rehabilitation and quality of life. Randomized, controlled study to compare the analgesic therapy with t... | |||||||||||||||||||||||
Medical condition: Hysterectomy with ASA 1-3, Prostatectomy with ASA 1-3, Nephrectomy with ASA 1-3 | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002203-32 | Sponsor Protocol Number: XRP6976J/3501 | Start Date*: 2006-02-15 | |||||||||||
Sponsor Name:sanofi-aventis group | |||||||||||||
Full Title: A Multicenter, Open-Label, Randomized, Phase III Trial Comparing Immediate Adjuvant Hormonal Therapy (ELIGARD®- leuprolide acetate) in Combination with TAXOTERE® (docetaxel) Administered Every Thre... | |||||||||||||
Medical condition: Prostate Cancer at High Risk of Relapse After Radical Prostatectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) BE (Completed) GB (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004704-34 | Sponsor Protocol Number: RECIR | Start Date*: 2021-03-16 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: Recovery from deep neuromuscular blockade using different sugammadex doses in elderly patients undergoing laparoscopic robot-assisted prostatectomy: a prospective, randomized, double-blind clinical... | |||||||||||||
Medical condition: Deep neuromuscular block in patients undergoing RALP under general anaesthesia | |||||||||||||
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Population Age: Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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