- Trials with a EudraCT protocol (121)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
121 result(s) found for: Mastectomy.
Displaying page 1 of 7.
EudraCT Number: 2010-023006-12 | Sponsor Protocol Number: 2010-362 | Start Date*: 2011-01-14 | |||||||||||
Sponsor Name:Professor Krzysztof Tadeusz Drzewiecki | |||||||||||||
Full Title: Lipofilling with MSC enriched fat, a permanent autologous filler? | |||||||||||||
Medical condition: Patients who have a need of reconstruction after surgery, eg. after mastectomy. The purpose of this clinical trial, is to make a reproducible and safe method for fat transplantation, that can be us... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006331-35 | Sponsor Protocol Number: PT-SM-10 | Start Date*: 2013-02-10 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Efficacy and safety of long term local anaesthetic intralesional infusion in patients with mammary carcinoma undergoing mastectomy with breast reconstruction: a randomized, double-blind study. | |||||||||||||
Medical condition: Post operative pain syndromes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000227-27 | Sponsor Protocol Number: DEXMAS01 | Start Date*: 2017-03-16 |
Sponsor Name:Eske Kvanner Aasvang | ||
Full Title: Effect of high versus low dose intravenous dexamethason on complications in the immediate postoperative setting after mastectomy - a randomized, double-blind, controlled trial | ||
Medical condition: Breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001557-46 | Sponsor Protocol Number: 01 | Start Date*: 2012-06-27 |
Sponsor Name:Sydvestjysk Sygehus, Esbjerg [...] | ||
Full Title: Perioperativ installation of ropivacain in mastectomy – with or without axillary lymph node dissection after sentinel node diagnostics or known lymph node metastasis – A double-blind, randomized cl... | ||
Medical condition: Unilateral mastectomy with or without axillary lymph node dissection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-005186-31 | Sponsor Protocol Number: 01062017 | Start Date*: 2018-06-06 | ||||||||||||||||
Sponsor Name:Department of Plastic Surgery, Breast and Burns Treatment | ||||||||||||||||||
Full Title: Fat Grafting with Ex-Vivo Expanded Adipose-Derived Stem Cells for Breast Reconstruction Following Mastectomy | ||||||||||||||||||
Medical condition: This study will include patients with genetic predisposition to development of breast cancer, who are offered prophylactic bilateral skin-sparring mastectomy. | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022749-74 | Sponsor Protocol Number: MASTEC-002 | Start Date*: 2011-06-14 | |||||||||||
Sponsor Name:CAROLINA IBAÑEZ LOPEZ | |||||||||||||
Full Title: ANALGESIA POSTOPERATORIA MEDIANTE LA INFUSIÓN DE UN ANESTESICO LOCAL EN EL LECHO QUIRURGICO TRAS MASTECTOMÍA RADICAL MODIFICADA | |||||||||||||
Medical condition: tratamiento del dolor en pacientes sometidas a mastectomia radical | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005775-16 | Sponsor Protocol Number: SUBLIME1 | Start Date*: 2012-06-19 | |||||||||||
Sponsor Name:Research and Development Department | |||||||||||||
Full Title: A randomised, double blind, placebo-controlled trial of continuous subpectoral local anaesthetic infusion for pain and shoulder function following mastectomy. | |||||||||||||
Medical condition: Post-operative pain following mastectomy surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001016-35 | Sponsor Protocol Number: ZUH-UMPR-MICB | Start Date*: 2019-05-29 | |||||||||||||||||||||
Sponsor Name:Associate Professor, Consultant Jens Børglum | |||||||||||||||||||||||
Full Title: The ultrasound-guided multiple-injection costotransverse block for mastectomy and primary reconstructive surgery. A double blind, randomised, placebo controlled trial. | |||||||||||||||||||||||
Medical condition: Postoperative pain following mastectomy and reconstructive surgery due to breast cancer. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002867-40 | Sponsor Protocol Number: 1 | Start Date*: 2011-11-22 | |||||||||||
Sponsor Name:Department of Anaesthesia | |||||||||||||
Full Title: Comparsion of continuous paravertebral blockade and continuous wound catheter infiltration for analgesia following mastectomy. | |||||||||||||
Medical condition: This study will involve the administration of levobupivicaine 0.125% and 0.25%, a local anaesthetic agent licensed for this purpose into the paravertebral space and into the surgical wound, to prov... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000100-41 | Sponsor Protocol Number: B-AP-ICG-IV | Start Date*: 2013-02-28 |
Sponsor Name:Jules Bordet Institute | ||
Full Title: Histological study of the (intravenously injected) Indocyanine Green (ICG) distribution in tumour bearing breasts and in axillary pieces of dissection | ||
Medical condition: breast cancer | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000513-37 | Sponsor Protocol Number: Z1031 | Start Date*: 2006-09-13 |
Sponsor Name:ACOSOG | ||
Full Title: A Randomised Phase III Trial comparing 16 to 18 weeks of neoadjuvant Exemestane (25mg daily), Letrozole (2.5mg), or Anastrozole(1mg) in postmenopausal Women with Clinical Stage II and III Estrogen... | ||
Medical condition: Breast Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002222-70 | Sponsor Protocol Number: Lidobreast | Start Date*: 2013-11-15 |
Sponsor Name:University Medical Centre St Radboud | ||
Full Title: Pilot study: Targeting the inflammatory response after breast cancer surgery with lidocaïne and dexamethasone | ||
Medical condition: Breast cancer patients who undergo surgery for treatment. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004443-20 | Sponsor Protocol Number: HP-LY-CL-2063 | Start Date*: 2018-05-07 | |||||||||||||||||||||
Sponsor Name:Herantis Pharma Plc | |||||||||||||||||||||||
Full Title: A Phase II, double-blind, placebo-controlled, randomized study to assess the efficacy, safety and tolerability of Lymfactin® (AdAptVEGF-C Adenoviral Vector) in combination with a surgical lymph nod... | |||||||||||||||||||||||
Medical condition: Secondary lymphedema associated with the treatment of breast cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FI (Prematurely Ended) SE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003575-18 | Sponsor Protocol Number: ICO-2020-06 | Start Date*: 2020-12-08 | |||||||||||
Sponsor Name:INSTITUT DE CANCEROLOGIE DE L'OUEST | |||||||||||||
Full Title: Impact of Neoadjuvant Hormonal Therapy on the Surgical Management of Extensive Ductal Carcinomas in Situ | |||||||||||||
Medical condition: Patients with extensive ductal carcinoma in situ with an indication for total mastectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (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: 2018-000910-39 | Sponsor Protocol Number: BRTR1 | Start Date*: 2018-12-13 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA UDINE | ||||||||||||||||||
Full Title: Efficacy of tranexamic acid in reducing post-operative bleeding in oncologic-reconstructive breast surgery | ||||||||||||||||||
Medical condition: Post-operative hematoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002774-51 | Sponsor Protocol Number: BrePainGenOxyc1 | Start Date*: 2013-06-27 |
Sponsor Name:Helsinki University Central Hospital | ||
Full Title: Genetic influences on pain and oxycodone consumption following mastectomy | ||
Medical condition: Women who are scheduled for breast cancer surgery. | ||
Disease: | ||
Population Age: | Gender: | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001484-64 | Sponsor Protocol Number: IBCSG 27-02/BIG 1-02/GEICAM 2002/04 | Start Date*: 2006-04-06 | |||||||||||
Sponsor Name:International Breast Cancer Study Group (IBCSG) | |||||||||||||
Full Title: Chemotherapy for Radically Resected Loco-regional Relapse A randomized clinical trial of adjuvant chemotherapy for radically resected loco-regional relapse of breast cancer Chemotherapy vs. Observa... | |||||||||||||
Medical condition: Patients with radically treated isolated local and/or regional recurrence of invasive breast cancer after mastectomy or breast-conserving surgery. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014823-22 | Sponsor Protocol Number: LISER-M | Start Date*: 2009-07-28 | |||||||||||
Sponsor Name:AZIENDA USL DI FORLI` | |||||||||||||
Full Title: Second biopsy of axillary sentinel node in the local recurrence of breast cancer after mastectomy and first negative sentinel node. Studio LiSeR - M | |||||||||||||
Medical condition: patients with first local recurrence of breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004872-17 | Sponsor Protocol Number: IC2020-04 | Start Date*: 2021-03-18 | ||||||||||||||||
Sponsor Name:INSTITUT CURIE | ||||||||||||||||||
Full Title: A Double-blind Randomized non-inferiority Trial of erector spinae block (ESP) versus paravertebral block (PVB) before Breast Cancer Surgery: Effects on acute Postoperative Pain | ||||||||||||||||||
Medical condition: Nervous Block erector spinae plane (ESP) or paravertebral block (PVB) preoperatively in women with breast adenocarcinoma without metastasis or breast in situ adenocarcinoma to by treated either by... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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