- Trials with a EudraCT protocol (44)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44 result(s) found for: Cervical Lymph Node.
Displaying page 1 of 3.
| EudraCT Number: 2018-001415-75 | Sponsor Protocol Number: RC31/17/0213 | Start Date*: 2019-11-15 | |||||||||||
| Sponsor Name:CHU de TOULOUSE | |||||||||||||
| Full Title: Induction chemotherapy followed by standard concurrent chemoradiotherapy in cervical cancer with para-aortic lymph node involvement: A phase III, multicenter, parallel-group randomized, controlled ... | |||||||||||||
| Medical condition: Cervical cancer with positive para-aortic lymph nodes | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003763-11 | Sponsor Protocol Number: CACZ885D2208 | Start Date*: 2016-06-15 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A 12-week, open-label, parallel-cohort study to evaluate the efficacy, safety and tolerability of canakinumab in pediatric IVIG-naïve or refractory patients with active Kawasaki disease | |||||||||||||
| Medical condition: Active Kawasaki disease | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) BE (Completed) DE (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001970-31 | Sponsor Protocol Number: HYBRID_ENDONODE | Start Date*: 2020-08-06 | |||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
| Full Title: Sentinel node in endometrial cancer using hybrid detection ([99mTc] Tc-albumin nanocoloid-ICG). Comparative pilot study between the lymphatic map derived from the cervical versus myometrial puncture. | |||||||||||||
| Medical condition: Patients with endometrial cancer who are going to undergo surgery for the primary tumor and lymph node study using lymphadenectomy and detection of the sentinel node | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005134-15 | Sponsor Protocol Number: NL75722.041.20 | Start Date*: 2021-03-25 | ||||||||||||||||
| Sponsor Name:University Medical Center Utrecht | ||||||||||||||||||
| Full Title: The bilateral sentinel node detection rate of fluorescent indocyanine green compared to 99mTc and blue dye in the sentinel node procedure in stage I-IIA cervical cancer | ||||||||||||||||||
| Medical condition: Sentinel lymph node procedure for patients with early-stage cervical cancer | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-003152-37 | Sponsor Protocol Number: MK3475-A18/ENGOT-cx11/GOG-3047 | Start Date*: 2020-05-28 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck &Co.,Inc | |||||||||||||
| Full Title: A Randomized, Phase 3, Double-Blind Study of Chemoradiotherapy With or Without Pembrolizumab for the Treatment of High-risk, Locally Advanced Cervical Cancer (KEYNOTE-A18 / ENGOT-cx11/GOG-3047) | |||||||||||||
| Medical condition: High-risk locally advanced cervical cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: NO (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) FR (Trial now transitioned) IE (Trial now transitioned) SE (Trial now transitioned) DE (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-003068-28 | Sponsor Protocol Number: 77946 | Start Date*: 2021-09-29 | |||||||||||||||||||||
| Sponsor Name:University Medical Center Utrecht | |||||||||||||||||||||||
| Full Title: Sentinel lymph node detection of cervical occult lymph node metastases in patients with parotid gland carcinoma by means of sentinel node biopsy using 68-galium-tilmanocept PET-CT. | |||||||||||||||||||||||
| Medical condition: The IMP will be used for the identification of sentinel lymph node(s) in patients with parotid gland carcinoma. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2014-002715-41 | Sponsor Protocol Number: P130934 | Start Date*: 2015-08-11 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: KAWAKINRA study, "A phase IIa multicenter trial to assess the efficacy and safety of Anakinra in patients with intraveinous immunoglobulin-resistant Kawasaki disease" | |||||||||||||
| Medical condition: Anakinra treatment is expected to reduce the early and long term mortality of patients with Kawasaki Disease (KD), by a rapid and sustained effect on vascular inflammation | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) FR (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-004844-20 | Sponsor Protocol Number: ADXS001-02 | Start Date*: 2017-05-08 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Advaxis, Inc | ||||||||||||||||||||||||||||||||||||||
| Full Title: Phase 3 Study of ADXS11-001 Administered Following Chemoradiation as Adjuvant Treatment for High Risk Locally Advanced Cervical Cancer: AIM2CERV (Advaxis IMmunotherapy 2 prevent CERVical recurrence) | ||||||||||||||||||||||||||||||||||||||
| Medical condition: High-risk locally advanced carcinoma of the cervix (HRLACC) following concurrent chemotherapy and radiation therapy. | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: ES (Prematurely Ended) PL (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-004310-18 | Sponsor Protocol Number: SPL-01-001 | Start Date*: 2019-10-07 | |||||||||||
| Sponsor Name:Saving Patients' Lives Medical B.V. | |||||||||||||
| Full Title: A confirmatory, prospective, open-label, single-arm, reader-blinded multi-centre phase 3 study to assess the diagnostic accuracy of Ferumoxtran-10-enhanced Magnetic Resonance Imaging (MRI) and unen... | |||||||||||||
| Medical condition: newly-diagnosed prostate cancer (PCA) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Prematurely Ended) NL (Prematurely Ended) BE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003622-33 | Sponsor Protocol Number: 2017/2608 | Start Date*: 2018-04-03 | ||||||||||||||||
| Sponsor Name:Gustave Roussy | ||||||||||||||||||
| Full Title: Randomized Phase II Trial Assessing the Inhibitor of Programmed Cell Death Ligand 1 (PD-L1) Immune Checkpoint Atezolizumab in Locally Advanced Cervical Cancer | ||||||||||||||||||
| Medical condition: Locally Advanced Cervical Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-005465-41 | Sponsor Protocol Number: CERVANTES | Start Date*: 2022-03-17 | |||||||||||
| Sponsor Name:CEEGOG reg. ass. | |||||||||||||
| Full Title: An international randomised trial of radical surgery followed by adjuvant (chemo)radiation versus no further treatment in patients with early-stage, intermediate-risk cervical cancer patients | |||||||||||||
| Medical condition: early-stage, intermediate-risk cervical cancer patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: CZ (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002665-30 | Sponsor Protocol Number: RENAISSANCE | Start Date*: 2016-01-11 |
| Sponsor Name:Krankenhaus Nordwest gGmbH | ||
| Full Title: Effect of chemotherapy alone vs. chemotherapy followed by surgical resection on survival and quality of life in patients with limited-metastatic adenocarcinoma of the stomach or esophagogastric jun... | ||
| Medical condition: limited-metastatic adenocarcinoma of the stomach or esophagogastric junction | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-003102-40 | Sponsor Protocol Number: M17CPF | Start Date*: 2018-11-01 | |||||||||||
| Sponsor Name:NKI-AVL | |||||||||||||
| Full Title: Neo-Adjuvant Chemotherapy and Conservative Surgery in Cervical Cancer to Preserve Fertility | |||||||||||||
| Medical condition: women ≥18 and ≤ 40 years with FIGO stage Ib1 cervical carcinoma with tumor measuring ≥ 2 cm and ≤ 4 cm on physical examination and imaging | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002155-15 | Sponsor Protocol Number: GEICO78-C | Start Date*: 2019-05-16 | |||||||||||
| Sponsor Name:Grupo Español de Investigación en Cáncer de Ovario (GEICO) | |||||||||||||
| Full Title: A randomized, open label, phase II trial of Anti-PD1, TSR-042, as maintenance therapy for patients with high-risk locally advanced cervical cancer after chemo-radiation | |||||||||||||
| Medical condition: Cervical cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-001290-78 | Sponsor Protocol Number: 007697 | Start Date*: 2012-01-17 |
| Sponsor Name:Barts Health NHS Trust | ||
| Full Title: Diagnostic accuracy of MRI, diffusion-weighted MRI, FDG-PET/CT and Fluoro-ethyl-choline PET/CT in the detection of lymph node metastases in surgically staged endometrial and cervical carcinoma | ||
| Medical condition: Endometrial and Cervical Cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-004638-99 | Sponsor Protocol Number: 2105xx1 | Start Date*: 2017-11-13 | |||||||||||||||||||||||||||||||
| Sponsor Name:Rigshospitalet, Department of Clinical Physiology, Nuclear Medicine and PET | |||||||||||||||||||||||||||||||||
| Full Title: Phase II trial: uPAR PET/CT and FDG PET/CT for preoperative staging of gynecological cancers | |||||||||||||||||||||||||||||||||
| Medical condition: gynecological cancers: Vulvar cancer endometrial cancer (uterine cancer) cervical cancer ovarian cancer | |||||||||||||||||||||||||||||||||
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| Population Age: Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2012-000576-42 | Sponsor Protocol Number: ICORG12-01 | Start Date*: 2012-04-05 | |||||||||||
| Sponsor Name:Cancer Trials Ireland | |||||||||||||
| Full Title: S1007, A Phase III, Randomized Clinical Trial of Standard Adjuvant Endocrine Therapy +/- Chemotherapy in Patients with 1-3 Positive Nodes, Hormone Receptor-Positive and HER2-Negative Breast Cancer ... | |||||||||||||
| Medical condition: Patients with 1-3 positive Nodes, Hormone Receptor-Positive and Her2-Negative Breast Cancer with recurrence Score (RS) of 25 or Less | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004944-37 | Sponsor Protocol Number: MK-3475-054-07 | Start Date*: 2015-09-22 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme LLC, a Subsidiary of Merck & Co. Inc | |||||||||||||
| Full Title: Adjuvant immunotherapy with anti-PD-1 monoclonal antibody Pembrolizumab (MK-3475) versus placebo after complete resection of high-risk Stage III melanoma: A randomized, double-blind Phase 3 trial o... | |||||||||||||
| Medical condition: Stage III melanoma (AJCC R0) with histologically confirmed cutaneous melanoma metastatic to lymph node, classified as (AJCC, 2010): Stage IIIA with metastasis > 1 mm; any Stage IIIB or IIIC (no in-... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) PT (Trial now transitioned) ES (Ongoing) DK (Trial now transitioned) AT (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) FI (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002322-11 | Sponsor Protocol Number: ARTemis | Start Date*: 2009-04-29 |
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust [...] | ||
| Full Title: ARTemis : Avastin® Randomised Trial with nEo-adjuvant cheMotherapy for patients wIth early breaSt cancer | ||
| Medical condition: HER2 negative invasive breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-002030-19 | Sponsor Protocol Number: ABCSG-24 | Start Date*: 2005-02-22 |
| Sponsor Name:AUSTRIAN BREAST CANCER STUDY GROUP | ||
| Full Title: A randomized phase III study comparing epirubicin, docetaxel and capecitabine + G-CSF to epirubicin and docetaxel + G-CSF as neoadjuvant treatment for early HER-2 negative breast cancer and compari... | ||
| Medical condition: early HER-2 breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
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