- Trials with a EudraCT protocol (21)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
21 result(s) found for: Breast reconstruction.
Displaying page 1 of 2.
EudraCT Number: 2022-001139-98 | Sponsor Protocol Number: IC2021-07 | Start Date*: 2022-06-13 | ||||||||||||||||
Sponsor Name:Institut Curie | ||||||||||||||||||
Full Title: Opioid-Free versus Opioid-Based Anaesthesia for secondary free-flap reconstruction surgery of the breast: A phase III multicentric randomized controlled study | ||||||||||||||||||
Medical condition: Anaesthesia during secondary free flap reconstruction surgery of the breast. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
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: 2020-002459-40 | Sponsor Protocol Number: BREAST-AB-01 | Start Date*: 2020-12-17 |
Sponsor Name:Rigshospitalet | ||
Full Title: Prophylactic treatment of breast implants with a solution of gentamicin, vancomycin and cefazolin antibiotics for women undergoing breast reconstructive surgery: a randomized controlled trial (The ... | ||
Medical condition: Implant-based breast reconstruction following mastectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004878-26 | Sponsor Protocol Number: 26842468452 | Start Date*: 2013-02-07 |
Sponsor Name:Karolinska University Hospital Solna | ||
Full Title: Antibiotic prophylaxis in patients undergoing primary or secondary breast reconstruction with implants, a randomized parallel two armed prospective clinical trial. | ||
Medical condition: The incidence of postoperative infections in patients with breast cancer or a history of breast cancer, after elective surgery with primary or secondary first-time breast reconstruction with implan... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Prohibited by CA) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000623-73 | Sponsor Protocol Number: LIDO | Start Date*: 2016-09-29 |
Sponsor Name:FUNDACIÓN INVESTIGACIÓN BIOMÉDICA HOSPITAL PUERTA DE HIERRO | ||
Full Title: LIDOCAINE IN ISCHEMIA-REPERFUSION INJURY FROM MICROSURGICAL BREAST RECONSTRUCTION. RANDOMISED UNICENTRIC, DOUBLE-BLIND, CLINICAL, CONTROLLED TRIAL. | ||
Medical condition: Ischemia-reperfusion injury from breast reconstruction microsurgical flaps. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000510-59 | Sponsor Protocol Number: 01012014 | Start Date*: 2014-08-11 | |||||||||||
Sponsor Name:Dept of Plastic Surgery, Breast Surgery & Burns | |||||||||||||
Full Title: Fat transplantation enriched with ex vivo expanded adipose-derived autologous mesenchymal stem cells in reconstruction of the breast. | |||||||||||||
Medical condition: The study will include participants with breast hypoplasia (International Classification of Diseases-10: DQ 838A). | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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: 2014-002616-16 | Sponsor Protocol Number: NL49061.031.14 | Start Date*: 2014-07-10 |
Sponsor Name:NKI-AVL | ||
Full Title: Pilot for high-resolution SPECT imaging of breast cancer lumpectomy specimens for 3D identification and quantification of resection margins | ||
Medical condition: Patients with breast cancer, IDC (n=3) and DCIS (n=3) scheduled for a lumpectomy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005114-33 | Sponsor Protocol Number: s57283 | Start Date*: 2015-03-10 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: Effectiveness of Botulinum Toxin Infiltration for treatment of upper limb dysfunctions after treatment for breast cancer | |||||||||||||
Medical condition: The aim of this study is to examine the effect of Botolinum Toxine infiltration in the pectoral muscle, in combination with an individual physical therapy programme, on pain and upper limb dysfunct... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000727-25 | Sponsor Protocol Number: 47582 | Start Date*: 2017-03-28 |
Sponsor Name:Isala Klinieken | ||
Full Title: The effect of ARTISS on latissimus dorsi donor site seroma formation after breast reconstruction: a randomised controlled trial. | ||
Medical condition: The aim of this study is to investigate the effect of the fibrin sealant ARTISS compared with our standard care on total volume of donor site seroma after harvesting a LD in immediate breast recons... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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: 2014-002119-41 | Sponsor Protocol Number: CE2261 | Start Date*: 2014-11-12 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: Influence of a new model of relative hypoxia on the evolution of erythropoietin and haemoglobin in patients undergoing breast reconstruction by a Deep Inferior Epigastric Perforator Flap. | |||||||||||||
Medical condition: Anaemia induced post operatively by hemodilution and surgical blood loss | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002635-28 | Sponsor Protocol Number: 69081 | Start Date*: 2019-10-14 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: The effect of hyperbaric oxygen therapy on breast cancer patients with late radiation toxicity | ||
Medical condition: Late radiation toxicity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003795-37 | Sponsor Protocol Number: CCR2644 | Start Date*: 2005-10-31 |
Sponsor Name:The Royal Marsden NHS Foundation Trust | ||
Full Title: Response to Parenteral Morphine and Oxycodone in Acute Pain. | ||
Medical condition: Post operative pain control in patients who have undergone major breast surgery for underlying breast cancer. Major breast surgery constitutes; • Mastectomy • Axillary clearance +/- wide local ex... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-005773-21 | Sponsor Protocol Number: IBMS-SPB | Start Date*: 2016-05-10 | |||||||||||
Sponsor Name:INSTITUTO DE INVESTIGACIÓN SANITARIA LA FE | |||||||||||||
Full Title: Impact of the serratus plane block in pain and the use of opioids in breast surgery | |||||||||||||
Medical condition: Patients undergoing oncological surgery and/or breast reconstruction surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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: 2022-000172-19 | Sponsor Protocol Number: DPAM | Start Date*: 2022-12-09 |
Sponsor Name:Consorci Sanitari Integral | ||
Full Title: Effect of 0.5% local lidocaine injection on the prevention of acute postoperative pain associated with breast surgery | ||
Medical condition: The reduction of acute postoperatory pain in female patients diagnosed with breast cancer and undergoing surgical treatment is investigated. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
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) |
EudraCT Number: 2011-004704-38 | Sponsor Protocol Number: GBG70 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:GBG Forschungs GmbH | |||||||||||||
Full Title: Dual blockage with Afatinib and Trastuzumab as neooadjuvant treatment for patients with lo-cally advanced or operable breast cancer receiving taxane-anthracycline containing chemo-therapy (DAFNE st... | |||||||||||||
Medical condition: Patients with HER2-positive early breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001028-21 | Sponsor Protocol Number: ABCSG_P01 | Start Date*: 2013-05-17 | |||||||||||
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | |||||||||||||
Full Title: P01 - A prospective, randomized, multicenter trial of additional radiochemotherapy to neoadjuvant chemotherapy in patients with locally advanced pancreatic adenocarcinoma | |||||||||||||
Medical condition: locally advanced pancreatic adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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