A Phase 1 Trial Of Safety And Initial Efficacy Of Vagal Nerve Blockade For Cancer-Induced Cachexia In Patients With Metastatic Pancreatic Adenocarcinoma
研究概览
详细说明
Primary Objective:
To determine the safety and tolerability of the OnVagus device in patients wearing it while receiving chemotherapy.
Secondary Objective:
To determine the rate of cachexia arrest, as defined by weight stabilization or gain
Exploratory Objectives:
To analyze the changes in chemokine (C-C motif) ligand 2 (CCL2), tumor necrosis factor α (TNFa), acetylcholine (ACh), Growth/differentiation factor 15 (GDF15), Lipocalin-2 (LCN2), and liver function tests (LFTs) while patients receive vagal blockade.
To determine the device's impact on progression-free survival (PFS) and overall survival (OS) between patients receiving vagal blockade.
研究类型
注册 (估计的)
阶段
- 阶段1
联系人和位置
学习联系方式
- 姓名:Brandon G. Smaglo, MD
- 电话号码:(713) 745-8763
- 邮箱:bgsmaglo@mdanderson.org
学习地点
-
-
Texas
-
Houston、Texas、美国、77030
- UT MD Anderson
-
接触:
- Brandon G. Smaglo, MD
- 电话号码:713-745-8763
- 邮箱:bgsmaglo@mdanderson.org
-
首席研究员:
- Brandon G. Smaglo, MD
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Patients with metastatic pancreatic cancer.
- Must have adenocarcinoma component (presence of combined histology is acceptable, as long as adenocarcinoma is present).
- Weight loss from baseline of at least 5% (Baseline weight can be anytime from diagnosis onward).
- Must have a tissue-based confirmation of diagnosis available. Tissue does not need to be a metastasis; primary tumor or prior surgery are acceptable sources.
- Must have had progression of disease after one prior line of therapy in the metastatic setting.
- Must be receiving or plan to receive another line of therapy in the metastatic setting. o If therapy is being administered outside MD Anderson, the patient is still eligible for this trial. o Enrollment onto a therapeutic clinical trial as this second line therapy is not explicitly excluded.
Must have triple ECG results available. Patients will be ineligible if they present: o Second- or third-degree block.
- Prolonged QT wave.
- Atrial fibrillation or flutter.
- Uncontrolled ventricular fibrillation or flutter.
- Premature ventricular contractions (PVC).
Exclusion Criteria:
Exclusion Criteria
- History of cervical vagotomy on the right side of neck.
- Known structural abnormalities on the right side of neck, including but not limited to situs inversus, bulky R-neck lymphadenopathy, etc., that in the investigators' opinion would lead to inability to correctly place the device onto the vagus nerve.
- Implanted electrical device that passes through the neck (e.g.: cranial implant with battery pack in chest, and wires running through the neck).
- Metal implants in the neck, including the cervical spine.
- Recent (6 months or less) nerve block or botox injections to the head or neck.
- Pain specifically localized to the treatment area, the right side of the neck.
- Prior severe cerebrovascular disease (e.g., intracranial aneurysm, intracranial hemorrhage, stroke).
- Prior severe cardiac disease, including but not limited to coronary artery disease (CAD), prior myocardial infarction (MI), uncontrolled congestive heart failure (CHF).
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Treatment with OnVagus device
Device will be applied by participant/caregiver daily for 30 min/day for 4 weeks; if well tolerated, 30 min twice per day for the following 4 weeks.
|
The transcutaneous LFVB (tLFVB), involves placing a superficial, transcutaneous device over the right vagus nerve.
The device can be self-applied, after participant/provider education on application is completed.
While applied, the device provides the low frequency vagal blockade intended to arrest the cachexia process.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Safety and Adverse Events (AEs)
大体时间:Through study completion; an average of 1 year.
|
ncidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
|
Through study completion; an average of 1 year.
|
合作者和调查者
调查人员
- 首席研究员:Brandon G. Smaglo, MD、UT MD Anderson
出版物和有用的链接
有用的网址
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- 2025-1708
- NCI-2026-05254 (其他标识符:NCI-CTRP Clinical Trials Registry)
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.