OncoSil Pancreatic Cancer Post-marketing Clinical Registry Italy
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 主要终点
- Safety and tolerability
研究概览
简要总结
The OSPRItaly Patient Registry has been developed to assess the performance and safety of the OncoSil™ device when used within the approved indication of unresectable, locally advanced pancreatic cancer, in combination with gemcitabine-based chemotherapy, within a real-world observational registry.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients who are eligible for and undergo OncoSil™ implantation at an eligible treatment facility according to the approved OncoSil™ System Instructions for Use (IFU), as part of their clinical care.
- •Patients who have completed and signed the Patient Informed Consent Form (PICF) for the OSPRItaly Patient Registry.
排除标准
- •Patients participating in an interventional clinical study (company or investigator-sponsored).
- •Use of an investigational agent at the time of enrolment.
结局指标
主要结局
Safety and tolerability
时间窗: Followed to death or to 24-months after the date of the last enrolled patient.
The analysis for safety within the real-world setting will be performed. The safety of OncoSil™ is defined by the Adverse Event profile. All safety summaries will be produced for the Intention-To-Treat (ITT) population. Adverse Device Effects will be coded using Medical Dictionary for Regulatory Activities (MedDRA). All Adverse Device Effects recorded during the Registry will be listed. Summary tables will be produced for Treatment Emergent Adverse Device Effects (TEADEs). The number and percentage of patients with device-related Adverse Events by system organ class (SOC) and preferred term will be tabulated. Similar summaries will be produced by severity of event (both mild, moderate or severe, CTCAE grade 1-4) and device relationship. In addition, summary tables will be produced for serious TEADEs and TEADEs associated with special interest acute/late radiation effects and or withdrawal.
Tumour response
时间窗: 1 year
Target (implanted) tumour response (local and distant)
Resection Rates
时间窗: Followed to death or 24 months after the date of the last enrolled patient
Surgical resection rates and outcome
Device implantation Performance
时间窗: 1 year
Safety of the implantation of OncoSil™ within the target tumour will be measured by means of procedure-related Adverse Events. Ease of administration and implantation related data from user questionnaires will be assessed.
Overall Survival
时间窗: Followed to death or to 24-months after the date of the last enrolled patient
Overall survival (OS) is defined as the time from enrolment to the date of death from any cause. Patients who are alive or permanently lost to follow-up at the cut-off date for the analysis will be censored at the last date the patient was known to be alive.
次要结局
未报告次要终点