A Pilot Study of REGENERA Implant in Localized Non- Malignant Breast Lesions Treated by Excision or Lumpectomy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Tensive SRL
- 入组人数
- 15
- 试验地点
- 2
- 主要终点
- Cumulative number of all Serious Adverse Events
研究概览
简要总结
The purpose of this First-in-Human pilot study is to evaluate the safety and performance of REGENERA breast implant in a selected cohort of patients with non- malignant breast lesions treated with excision or lumpectomy in whom the tissue removed is replaced by REGENERA.
详细描述
This is a pre-market, single center, interventional, open label, non-comparative, pilot first-in-human study on adult female patients with localized non-malignant breast lesion. This study will include an enrollment period of 12 months and 6 months study duration per patient.
The primary objective of this study is to demonstrate the safety profile of a new breast implant (REGENERA) in excision or lumpectomy of non-malignant breast lesions.
The secondary objectives of this study are:
-
To assess the safety of the implant procedure
-
To assess the feasibility of the implant procedure
-
To evaluate the performance of REGENERA breast implant:
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In replacing the removed tissue
-
In potential interference with current diagnostic standard of care imaging procedures
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On patient's quality of life and satisfaction
-
On investigator's satisfaction.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 85 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Female patients aged 20-85 years
- •Patients eligible for excision or lumpectomy, as per current surgical guidelines
- •Volume deficit compatible with an implant volume of 70 cc
- •Adequate hematopoietic functions
- •Good general health and mentally sound
- •Confirmation of non-malignant lesion (B2 and B3) with no discordance between biopsy and radiological imaging
- •Patients able and willing to give written informed consent form
排除标准
- •Pregnant or breastfeeding women or women who have nursed a child three months within enrolment in the study
- •Non-malignant lesions (B2 and B3) with discordance between biopsy and radiological imaging
- •Infection of the surgical site confirmed pre-operatively by clinical examination
- •Acute or chronic severe renal insufficiency (creatinine values < 180 μmol/L)
- •History of severe asthma or allergies (including to anaesthetics or contrast media)
- •Autoimmune disease
- •Subject with actual concomitant malignancies, lobular neoplasm, metastatic breast carcinoma, sarcoma, malignant phyllodes lesions, or Paget's disease
- •Subject who are known to be carriers of BCRA mutation
- •Inability to undergo MRI or allergy to contrast media
- •Systemic infections in active phase
- •Immunocompromised patients (HIV)
- •Subjects who have participated in another study within the past 3 months
- •Patients who received immunosuppressant therapy in the last 3 months
- •Non-collaborative patients (severe physical disabilities or psychiatric disorders, as per specialist opinion).
结局指标
主要结局
Cumulative number of all Serious Adverse Events
时间窗: at 6 months from implantion of the device
Cumulative number of Serious Adverse Events collected throughout the study and associated with the REGENERA implant device (Adverse Device Effects)
次要结局
- Patient Quality of Life measured through Breast-Q questionnaire(at 1 month from the implantation of the device (Day 0), 6 months from Day 0 versus 2 weeks before Day 0)
- Cumulative number of all Adverse Events associated with the surgical procedure(at 6 months from the implantation of the device)
- Measurement of changes in breast appeareance before and after surgery through antropomorphic chest parameters(at 2 weeks before the implantation of the device (Day 0), 1 week from Day 0, 3 months from Day 0, 6 months from Day 0)
- Measurement of the reduction of reliability of the currently used diagnostic imaging techniques(at 1 week from the implantation of the device (Day 0), 2 weeks from Day 0, 1 month from Day 0, 3 months from Day 0 and 6 months from Day 0)
- Patient pain measurement through a Visual Analogue Scale(at 2 weeks before the implantation of the device (Day 0), Day 0, 1 week from Day 0, 2 weeks from Day 0, 1 month from Day 0, 3 months from Day 0 and 6 months from Day 0)
- Measure of the Investigator's satisfaction on the implantation procedure, through a Visual Analogue Scale (VAS) and an ad-hoc questionnaire(implantation satisfaction (VAS + ad-hoc questionnaire) at the implantation of the device (Day 0) and REGENERA performance (VAS) at 6 months from Day 0)