- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07700212
A Phase 1 Trial Of Safety And Initial Efficacy Of Vagal Nerve Blockade For Cancer-Induced Cachexia In Patients With Metastatic Pancreatic Adenocarcinoma
연구 개요
상세 설명
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.
연구 유형
등록 (추정된)
단계
- 1단계
연락처 및 위치
연구 연락처
- 이름: Brandon G. Smaglo, MD
- 전화번호: (713) 745-8763
- 이메일: bgsmaglo@mdanderson.org
연구 장소
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Texas
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Houston, Texas, 미국, 77030
- UT MD Anderson
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연락하다:
- Brandon G. Smaglo, MD
- 전화번호: 713-745-8763
- 이메일: bgsmaglo@mdanderson.org
-
수석 연구원:
- Brandon G. Smaglo, MD
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
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).
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: 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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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Safety and Adverse Events (AEs)
기간: 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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공동 작업자 및 조사자
수사관
- 수석 연구원: Brandon G. Smaglo, MD, UT MD Anderson
간행물 및 유용한 링크
유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- 2025-1708
- NCI-2026-05254 (기타 식별자: NCI-CTRP Clinical Trials Registry)
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
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