- Trials with a EudraCT protocol (109)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
109 result(s) found for: Sentinel lymph node.
Displaying page 2 of 6.
EudraCT Number: 2019-001088-58 | Sponsor Protocol Number: SELLY | Start Date*: 2020-03-19 | ||||||||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | ||||||||||||||||||
Full Title: SEntinel Lymph node in EarLY ovarian cancer: the SELLY protocol | ||||||||||||||||||
Medical condition: ADVANCED OVARIAN CANCER | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000988-25 | Sponsor Protocol Number: version4 | Start Date*: 2012-04-27 |
Sponsor Name:Gateshead Health NHS Trust Research & Development | ||
Full Title: To determine the feasibility of using Microbubble technology to detect sentinel nodes in vulvar cancer. | ||
Medical condition: Early stage vulvar cancer with no clinial or radiological evidence of lymph node metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005350-79 | Sponsor Protocol Number: NN028-1801 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A single arm, single-centre, open-label, exploratory trial of recombinant Interleukin-21 administered subcutaneously for 4 weeks as neo-adjuvant treatment prior to sentinel lymph node/complete lymp... | |||||||||||||
Medical condition: Recombinant Interleukin-21 administered subcutaneously for 4 weeks as neo-adjuvant treatment prior to sentinel lymph node/complete lymph node dissection followed by 8 weeks of adjuvant treatment in... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003179-20 | Sponsor Protocol Number: 71065 | Start Date*: 2020-03-23 |
Sponsor Name:Meander Medical Centre | ||
Full Title: ‘A pilot study to assess the safety and feasibility of fluorescent sentinel lymph node identification in colon carcinoma using Indocyanine green’ | ||
Medical condition: Colon carcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004914-32 | Sponsor Protocol Number: NL71558.041.19 | Start Date*: 2020-03-12 | |||||||||||||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||||||||||||
Full Title: Sentinel lymph node (SLN) detection in early oral cancer using Gallium-68-Tilmanocept PET-CT | |||||||||||||||||||||||
Medical condition: The IMP will be used for the identification of sentinel lymph nodes in patients with early-stage oral squamous cell carcinoma and a clinically negative neck (T1-3N0M0). | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Temporarily Halted) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005011-17 | Sponsor Protocol Number: 7TNANO1 | Start Date*: 2015-02-24 |
Sponsor Name:Radboudumc | ||
Full Title: Nano MRI on 7 Tesla: A technical validation study in rectal and breast cancer | ||
Medical condition: Lymph node metastases in rectal cancer, breast cancer and cancer in general | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2011-005219-98 | Sponsor Protocol Number: PH3-01 | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:Galena Biopharma, Inc | |||||||||||||
Full Title: Prevention of Recurrence in Early-Stage, Node-Positive Breast Cancer with Low to Intermediate HER2 Expression with NeuVax™ Treatment (PRESENT) | |||||||||||||
Medical condition: Operable early-stage, node-positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000709-18 | Sponsor Protocol Number: T2017-7 | Start Date*: 2018-07-02 |
Sponsor Name:Bernhoven | ||
Full Title: The effect of erector spinae block on postoperative pain and opioid use in patients undergoing breast cancer surgery with sentinel node dissection | ||
Medical condition: Patients undergoing unilateral (modified) mastectomy with sentinel node dissection for breast cancer | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016743-18 | Sponsor Protocol Number: ICG10 | Start Date*: 2010-02-02 |
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | ||
Full Title: A feasibility study of indocyanine green (ICG) fluorescence mapping for sentinel lymph node detection in early breast cancer | ||
Medical condition: Primary breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001474-25 | Sponsor Protocol Number: SVM9122 | Start Date*: 2012-01-02 |
Sponsor Name:Klinik für Dermatologie, Venerologie und Allergologie; Charité - Universitätsmedizin Berlin | ||
Full Title: A single-centre, single arm, open-label, exploratory trial of Interleukin-2 administered subcutaneously as neo-adjuvant treatment prior to sentinel lymph node biopsy(SLNB)/complete lymph node disse... | ||
Medical condition: The trial is planned in a neo-adjuvant setting for a 4-weeks period in Melanoma patients with stage III. The stage is to be discovered by ultrasound and veriefied by fine needle punctere and cytology. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-004822-19 | Sponsor Protocol Number: ICORG 05-11/NSABP B-38 | Start Date*: 2006-02-15 |
Sponsor Name:ICORG the all Ireland Co-operative Oncology Research Group | ||
Full Title: A Phase III, adjuvant trial comparing three chemotherapy regimens in women with node positive breast cancer: Docetaxel/Doxorubicin/Cyclophosphamide (TAC); Dose-Dense (DD) Doxorubicin/Cyclophosphami... | ||
Medical condition: Early stage node positive breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002597-32 | Sponsor Protocol Number: AGO/2019/003 | Start Date*: 2020-03-16 | |||||||||||
Sponsor Name:University Hospital Ghent | |||||||||||||
Full Title: Dynamics and tracer distribution of Tilmanocept using combined subareolar and peritumoral injection technique for scintigraphic sentinel lymph node detection in early stage breast cancer. | |||||||||||||
Medical condition: Early stage breast cancer (T1, T2) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011079-57 | Sponsor Protocol Number: BICG26UMCG-NIRF | Start Date*: 2009-05-28 | ||||||||||||||||
Sponsor Name:University Medical Center Groningen | ||||||||||||||||||
Full Title: Evaluation of Indocyanine Green (ICG) enhanced Near-InfraRed Fluorescence (NIRF) Imaging for Intra-Operative Sentinel Lymph Node (SLN) detection in Breast Surgery. | ||||||||||||||||||
Medical condition: Women above the age of 21 with core biopsy or cytology proven breast cancer stage I and II, eligible for lumpectomy and sentinel lymph node procedure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001230-34 | Sponsor Protocol Number: CA209-76K | Start Date*: 2019-08-06 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind Study of Adjuvant Immunotherapy with Nivolumab versus Placebo after Complete Resection of Stage IIB/C Melanoma (CheckMate 76K: CHECKpoint pathway and nivoluMAb ... | |||||||||||||
Medical condition: Completely resected Stage IIb/c melanoma subjects. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) AT (Trial now transitioned) CZ (Ongoing) SE (Trial now transitioned) NO (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) BE (Trial now transitioned) GR (Trial now transitioned) FI (Trial now transitioned) DK (Trial now transitioned) NL (Ongoing) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) Outside EU/EEA RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003828-21 | Sponsor Protocol Number: 71617 | Start Date*: 2020-02-10 |
Sponsor Name:St Antonius Hospital | ||
Full Title: Identification of sentinel lymph nodes in breast cancer patients through non-invasively and percutaneously fluorescent imaging using indocyanine green | ||
Medical condition: Axillar staging in breast cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003194-28 | Sponsor Protocol Number: PULSION-001 | Start Date*: 2011-10-24 | |||||||||||
Sponsor Name:PULSION Medical Systems SE | |||||||||||||
Full Title: Determination of the sensitivity of ICG fluorescence technique for the detection of Sentinel Lymph Nodes in breast cancer – a monocenter, prospective open-label clinical trial | |||||||||||||
Medical condition: Breast cancer with indicated sentinel lymph node biopsy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000424-18 | Sponsor Protocol Number: ICTUC/32/2012 | Start Date*: 2012-10-26 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: A study to assess near infrared laparoscopy with indocyanine green (ICG) for intraoperative lymphatic imaging and sentinel lymph node identification during standard surgical resection for colonic c... | |||||||||||||
Medical condition: Bowel cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003578-28 | Sponsor Protocol Number: 2013070001 | Start Date*: 2013-10-21 | |||||||||||
Sponsor Name:Andreas Kjær | |||||||||||||
Full Title: The intraoperative use of fluorescent tracers and multimodal imaging techniques in treatment of head and neck cancer | |||||||||||||
Medical condition: oral cavity cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004943-32 | Sponsor Protocol Number: ICORG1124NSABPB47 | Start Date*: 2011-12-13 | |||||||||||
Sponsor Name:Irish Clinical Oncology Research Group CLG, trading as Cancer Trials Ireland | |||||||||||||
Full Title: ICORG 11-24-NSABP PROTOCOL B-47 A Randomized Phase III Trial of Adjuvant Therapy Comparing Chemotherapy Alone (Six Cycles of Docetaxel Plus Cyclophosphamide or Four Cycles of Doxorubicin Plus Cy... | |||||||||||||
Medical condition: Node positive, or high risk node negative invasive breast cancer in patients that are HER 2 low | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006181-42 | Sponsor Protocol Number: RAD_USPALS_01 | Start Date*: 2007-03-15 | |||||||||||
Sponsor Name:UMC St Radboud | |||||||||||||
Full Title: The use of USPIO enhanced MRI in the assessment of axillary lymph node status in patients with invasive breast cancer | |||||||||||||
Medical condition: The presence of axillary metastasis in patients with proven invasive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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