- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
49 result(s) found for: Manipulation.
Displaying page 1 of 3.
| EudraCT Number: 2006-004587-30 | Sponsor Protocol Number: GOS/002/C | Start Date*: 2006-11-04 |
| Sponsor Name:NOVOSIS AG | ||
| Full Title: An open label, parallel group, Phase III clinical study in patients with advanced prostate cancer suitable for hormonal manipulation to demonstrate the non-inferiority of a new three-month Novosis ... | ||
| Medical condition: prostate cancer suitable for hormonal manipulation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: HU (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-024649-61 | Sponsor Protocol Number: POXY11 | Start Date*: 2011-04-05 | |||||||||||
| Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
| Full Title: Pilot study: performance of the Progensa PCA3 test in post-oxytocin urine specimens | |||||||||||||
| Medical condition: Healthy volunteer trial: intended indication for product is to mobilize prostate cells in urethra for PCA3 test. | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002389-13 | Sponsor Protocol Number: | Start Date*: 2005-11-23 |
| Sponsor Name:Moorfields Eye Hospital | ||
| Full Title: Endothelial Lamellar Keratoplasty (ELK) with Tisseel adhesive. | ||
| Medical condition: Corneal endothelial failure, from Fuchs' corneal endothelial dystrophy, aphakic and pseudophakic bullous keratopathy and other causes. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-002376-95 | Sponsor Protocol Number: RRK3535 | Start Date*: 2009-01-05 |
| Sponsor Name:University Hospital Birmingham NHS Foundation Trust | ||
| Full Title: Myocardial protection with Perhexiline in Left Ventricular Hypertrophy | ||
| Medical condition: Patients with left ventricular hypertrophy undergoing aortic valve surgery (with or without coronary artery surgery) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-002021-35 | Sponsor Protocol Number: ANR-1/14 | Start Date*: 2014-09-23 |
| Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori | ||
| Full Title: Decurarization After Thoracic Anesthesia - A prospective multicenter double-blind randomized trial comparing sugammadex vs neostigmine reversal after thoracic anesthesia | ||
| Medical condition: Neuromuscular block is commonly adopted during general anesthesia to facilitate tracheal intubation, mechanical ventilation and surgical manipulation. At the end of anesthesia it very important to ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-018735-18 | Sponsor Protocol Number: AMW/002/C | Start Date*: 2011-02-07 |
| Sponsor Name:AMW GmbH | ||
| Full Title: An open label, multiple dose Phase III clinical study in patients with prostate cancer to investigate the clinical efficacy and safety of a new GnRH implant (AMW Goserelin 10.8 mg Implant) applied ... | ||
| Medical condition: prostate cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-001687-37 | Sponsor Protocol Number: LEX/001/C | Start Date*: 2008-07-08 | |||||||||||
| Sponsor Name:Novosis AG | |||||||||||||
| Full Title: An open label, parallel group phase III clinical study in patients with prostate cancer to demonstrate the non-inferiority of a new Novosis Leuprorelin 10.72 mg implant versus the reference product... | |||||||||||||
| Medical condition: Male patients with carcinoma of the prostate aged 18 years and more and suitable for hormonal manipulation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-000926-38 | Sponsor Protocol Number: LEU/001/C | Start Date*: 2008-05-08 | |||||||||||
| Sponsor Name:Novosis AG | |||||||||||||
| Full Title: An open label, parallel group, multiple dose Phase III clinical study in patients with prostate cancer to demonstrate the non-inferiority of a new Novosis Leuprorelin 3.57 mg implant versus the ref... | |||||||||||||
| Medical condition: Patients who have advanced carcinoma of the prostate suitable for hormonal manipulation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-010163-16 | Sponsor Protocol Number: 08/0285 | Start Date*: 2009-06-05 | ||||||||||||||||
| Sponsor Name:University College London | ||||||||||||||||||
| Full Title: Bile salt manipulation as a novel treatment for Crohn’s disease: a single centre open label pilot study of atorvastatin and colesevalam in patients with active ileal Crohn’s disease | ||||||||||||||||||
| Medical condition: Active Crohn's disease affecting the ileum | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-004823-66 | Sponsor Protocol Number: ELTCAN1 | Start Date*: 2019-04-17 | |||||||||||
| Sponsor Name:Radboudumc | |||||||||||||
| Full Title: Early-life stress, the endocannabinoid system, and fear memory extinction | |||||||||||||
| Medical condition: healthy volunteers | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001656-22 | Sponsor Protocol Number: 1601 | Start Date*: 2016-11-17 | |||||||||||
| Sponsor Name:Ziekenhuis Oost Limburg | |||||||||||||
| Full Title: The utility of liposomal bupivacaine for anesthesia and analgesia in patients treated with collagenase for the release of Dupuytren’s contracture: A randomized controlled trial. | |||||||||||||
| Medical condition: Introduction of collagenase clostridium histolyticum injection for the treatment of Dupuytren’s contractures. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-005222-19 | Sponsor Protocol Number: BREATH | Start Date*: 2016-07-14 | |||||||||||
| Sponsor Name:Leiden University Medical Center | |||||||||||||
| Full Title: Effect of neuromuscular blockade and reversal by sugammadex versus neostigmine on breathing when hypoxic or hypercapnic in volunteers | |||||||||||||
| Medical condition: Postoperative ventilatory control | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000091-10 | Sponsor Protocol Number: 2014121566 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Rigshospitalet, department of surgical Gastroenterology, C-Tx | |||||||||||||
| Full Title: RCT-comparison of two hemostatic devices (Hemopath vs. Tachosil) in liver resection. | |||||||||||||
| Medical condition: Bleeding during liver resection and the efficacy of 2 types of hemostatic patches on this, thus all diagnosis' that require liver resection. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-005728-17 | Sponsor Protocol Number: HOP LITE | Start Date*: 2006-11-02 | |||||||||||
| Sponsor Name:AZIENDA PROVINCIALE PER I SERVIZI SANITARI DELLA PROVINCIA AUTONOMA DI TRENTO | |||||||||||||
| Full Title: Hormone-refractory Prostate cancer first Line Intermittent Taxotere and Estramustine. | |||||||||||||
| Medical condition: Prostate cancer. | |||||||||||||
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| Population Age: Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003740-39 | Sponsor Protocol Number: URO-CHUAC-BPSat-001. | Start Date*: 2016-04-12 | |||||||||||
| Sponsor Name:Jose Luis Ponce Díaz-Reixa | |||||||||||||
| Full Title: Open randomized clinical trial to examine individual pain tolerance in the use of two anesthetic techniques to perform saturation prostate biopsy . | |||||||||||||
| Medical condition: Prostate biopsy anesthesia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-011059-27 | Sponsor Protocol Number: RBHP 2009 BONNIN | Start Date*: 2009-06-17 |
| Sponsor Name:CHU Clermont-Ferrand | ||
| Full Title: Etude des effets de l’adjonction de clonidine au mélange anesthésique local + opiacé destiné à l’infusion péridurale autocontrôlée pour l’analgésie du travail obstétrical (lévobupivacaïne 0,568 mg/... | ||
| Medical condition: parturiente en cours de travail obstétrical | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-003231-20 | Sponsor Protocol Number: BE-02-RG-186 | Start Date*: 2008-11-26 | |||||||||||
| Sponsor Name:KULeuven | |||||||||||||
| Full Title: Adherence Measurement in stable renal transplant patients following conversion form Prograft to advagraf | |||||||||||||
| Medical condition: Renal transplant patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003778-30 | Sponsor Protocol Number: DRO-200/III/21/1 | Start Date*: 2021-12-29 |
| Sponsor Name:Drossapharm AG | ||
| Full Title: Randomized, controlled, multi-center trial to evaluate the efficacy and safety of Lixim 70 mg wirkstoffhaltiges Pflaster (etofenamate 70 mg medicated plaster) vs. placebo in the local symptomatic a... | ||
| Medical condition: Acute strains, sprains or bruises of soft tissues following blunt trauma, e.g. sports injuries | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-003408-15 | Sponsor Protocol Number: DMEC | Start Date*: 2021-06-14 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: A randomized clinical two-arm trial comparing inflammation and cystoid macular edema for the medication regimens postoperative topical NSAIDs and steroids to only postoperative topical steroids in ... | ||
| Medical condition: Corneal disease/opacification treated with corneal endothelial transplantation (DSAEK or DMEK surgery), and the medical treatment is anti-inflammatory eye drops to treat (and prevent) intraocular i... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003792-19 | Sponsor Protocol Number: FOS-PROST-001 | Start Date*: 2021-03-04 |
| Sponsor Name:Hospital Universitari Mutua Terrassa | ||
| Full Title: Fosfomycin as an oral alternative treatment for acute bacterial prostatitis due to multi-drug resistant Escherichia coli. Pilot study | ||
| Medical condition: Acute bacterial prostatitis due to multi-drug resistant Escherichia coli | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
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