A Phase 1 Trial Of Safety And Initial Efficacy Of Vagal Nerve Blockade For Cancer-Induced Cachexia In Patients With Metastatic Pancreatic Adenocarcinoma
調査の概要
詳細な説明
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.
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Brandon G. Smaglo, MD
- 電話番号:(713) 745-8763
- メール:bgsmaglo@mdanderson.org
研究場所
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Texas
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Houston、Texas、アメリカ、77030
- UT MD Anderson
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コンタクト:
- Brandon G. Smaglo, MD
- 電話番号:713-745-8763
- メール:bgsmaglo@mdanderson.org
-
主任研究者:
- Brandon G. Smaglo, MD
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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).
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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.
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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.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Safety and Adverse Events (AEs)
時間枠:Through study completion; an average of 1 year.
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ncidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
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Through study completion; an average of 1 year.
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協力者と研究者
捜査官
- 主任研究者:Brandon G. Smaglo, MD、UT MD Anderson
出版物と役立つリンク
便利なリンク
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- 2025-1708
- NCI-2026-05254 (その他の識別子:NCI-CTRP Clinical Trials Registry)
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
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