- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10 result(s) found for: Thermal imaging.
Displaying page 1 of 1.
| EudraCT Number: 2006-005630-21 | Sponsor Protocol Number: RG_06-180 | Start Date*: 2009-04-09 |
| Sponsor Name:University of Birmingham [...] | ||
| Full Title: The effect of Pregabalin on Pain progressing in Painful Diabetic Neuropathy | ||
| Medical condition: Diabtes and its complications, painful neuropathy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-013468-37 | Sponsor Protocol Number: Protocol code BA7 | Start Date*: 2010-09-29 | ||||||||||||||||
| Sponsor Name:Royal National Hospital for Rheumatic Disease | ||||||||||||||||||
| Full Title: A short-term open-label single site pilot study evaluating the use of asasantin retard therapy in the management of Raynaud’s phenomenon. | ||||||||||||||||||
| Medical condition: Primary Raynaud's Phenomenon and Systemic Sclerosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-000176-19 | Sponsor Protocol Number: IP-IIO-622 | Start Date*: 2023-01-10 | |||||||||||||||||||||
| Sponsor Name:Immunophotonics Inc. | |||||||||||||||||||||||
| Full Title: Intratumoral injection of IP-001 following thermal ablation in patients with advanced solid tumors. A multicenter Phase 1b/2a trial in colorectal cancer, non-small cell lung cancer, and soft tissue... | |||||||||||||||||||||||
| Medical condition: Colorectal cancer, non-small cell lung cancer, and soft tissue sarcoma patients | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2012-005627-32 | Sponsor Protocol Number: IIVOP | Start Date*: 2014-06-12 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | |||||||||||||
| Full Title: A randomised, double blind, placebo controlled crossover study of the influence of the HCN channel blocker ivabradine in a healthy volunteer pain model - an enriched population study | |||||||||||||
| Medical condition: Neuropathic Pain | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000141-52 | Sponsor Protocol Number: Landscaping_2017 | Start Date*: 2017-04-03 | |||||||||||
| Sponsor Name:Asbjørn Mohr Drewes | |||||||||||||
| Full Title: The effect of tapentadol on the human pain system: A study based on advanced neurophysiology and imaging techniques to illustrate the mechanism of tapentadol and oxycodone in the central, autonomic... | |||||||||||||
| Medical condition: Healthy volunteers - pain | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001455-37 | Sponsor Protocol Number: 1331TMF | Start Date*: 2011-12-21 | |||||||||||
| Sponsor Name:Department of Radiology, Oslo University Hospital, Norway | |||||||||||||
| Full Title: Prospective randomized interventional study. Compare the effect of bleomycin and Tetradecyl Sodium Sulphate (Fibrovein) in the treatment of venous malformations. Clinical neurological and neurophys... | |||||||||||||
| Medical condition: Venous malformation | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002214-17 | Sponsor Protocol Number: NL78220.029.21 | Start Date*: 2023-04-24 | ||||||||||||||||
| Sponsor Name:Amsterdam University Medical Centers | ||||||||||||||||||
| Full Title: COLLISION RELAPSE trial - Recurrent colorectal liver metastases: repeat local treatment +/- neoadjuvantsystemic therapy - a phase III prospective randomized controlled trial | ||||||||||||||||||
| Medical condition: Recurrent colorectal liver metastases | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-001907-33 | Sponsor Protocol Number: S2472 | Start Date*: 2022-07-21 | |||||||||||
| Sponsor Name:Biocompatibles UK Ltd, a wholly owned indirect subsidiary of Boston Scientific Corporation | |||||||||||||
| Full Title: An Open-Label, Prospective, Multi-Center, Randomized Clinical Trial To Evaluate The Efficacy and Safety Of TheraSphere™ followed by Durvalumab (Imfinzi®) With Tremelimumab, Versus TheraSphere™ Alon... | |||||||||||||
| Medical condition: hepatocellular carcinoma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Temporarily Halted) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004425-41 | Sponsor Protocol Number: ESN364-UF-02 | Start Date*: 2015-01-21 | |||||||||||
| Sponsor Name:Euroscreen S.A | |||||||||||||
| Full Title: A Phase IIa, Double-Blind, Placebo-Controlled, Study of ESN364 Administered for 12 Weeks to Evaluate Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics in Women Presenting With ... | |||||||||||||
| Medical condition: Uterine Fibroids | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001049-24 | Sponsor Protocol Number: ACW0002 | Start Date*: 2017-04-03 | |||||||||||
| Sponsor Name:Actinogen Medical | |||||||||||||
| Full Title: XanADu: A Phase II, Double-Blind, 12-Week, Randomised, Placebo-Controlled Study to Assess the Safety, Tolerability and Efficacy of Xanamem™ in Subjects with Mild Dementia due to Alzheimer’s Disea... | |||||||||||||
| Medical condition: Mild Dementia due to Alzheimer’s Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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