Transcutaneous Auricular Vagal Neuromodulation Therapy (AVNT™) in Chronic Kidney Disease Autonomic Dysfunction
Feasibility and Preliminary Efficacy of Transcutaneous Auricular Vagal Neuromodulation Therapy (AVNT™) in Chronic Kidney Disease Autonomic Dysfunction: A Randomized, Sham-Controlled Pilot Trial (Parasym-CKD)
The purpose of this pilot study is to establish the feasibility of home-based Auricular Vagal Neuromodulation Therapy (AVNT™) in Chronic Kidney Disease (CKD) patients, generate preliminary efficacy data on autonomic function outcomes, and explore whether timing variation influences treatment response.
研究概览
地位
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Qandeel Soomro, MD, MS
- 电话号码:929-573-1168
- 邮箱:Qandeel.Soomro@nyulangone.org
研究联系人备份
- 姓名:David Moran
- 电话号码:212-263-4072
- 邮箱:David.Moran@nyulangone.org
学习地点
-
-
New York
-
New York、New York、美国、10016
- NYU Langone Health
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Age ≥18 years at time of informed consent
- Documented Chronic Kidney Disease (CKD) stage G3-G5 (estimated Glomerular Filtration Rate (eGFR) 15-59 mL/min/1.73 m²), not on maintenance dialysis, based on eGFR or clinical documentation
- Patients at New York University (NYU) clinics who meet criteria
- Non NYU patients reaching out study team via iConnect
- Clinically stable: No hospitalization, acute kidney injury, or acute illness requiring medical intervention within prior 4 weeks
- Stable dosing of autonomically active medications: participants taking beta-blockers, other rate-controlling agents, anticholinergics, or sympathomimetics must be on a stable dose for ≥4 weeks before baseline with no anticipated changes during the study. Use of these agents is recorded and included as a covariate in analyses of heart-rate-based endpoints. Autonomically active medications: agents that materially affect heart rate, blood pressure, or autonomic tone - beta-blockers, non-dihydropyridine calcium-channel blockers, alpha-blockers, central sympatholytics (e.g., clonidine), midodrine, fludrocortisone, anticholinergics, sympathomimetics/stimulants, serotonin-norepinephrine reuptake inhibitors (SNRIs)/selective serotonin reuptake inhibitors (SSRIs), and diuretics are recorded with agent, dose, and timing, must be stable for ≥4 weeks before baseline with no anticipated change during the study, and are included as covariates. Home measurements are taken at a consistent time relative to the participant's usual dosing.
Exclusion Criteria:
-
Implantable cardioverter-defibrillator (ICD) or other implanted cardiac device
-
Known severe coronary disease (≥70% stenosis in major vessel) or myocardial infarction within past 5 years
-
Hospitalized within 4 weeks
-
Syncope or unexplained loss of consciousness within past 12 months
-
Uncontrolled arrhythmia (atrial fibrillation with resting heart rate >110 bpm, recent runs of sustained ventricular tachycardia or supraventricular tachycardia) within 3 months.
-
Severe bradycardia (<40 bpm at rest, symptomatic) , or second- or third-degree atrioventricular (AV) block without a functioning pacemaker
-
Neurological/Anatomical Exclusions:
-
History of vagotomy (surgical cutting of vagus nerve)
-
Trigeminal neuralgia within 1 year
-
Epilepsy or seizure disorder (unless well-controlled defined as seizure free with stable dose of medication for ≥2 years)
-
Dementia or cognitive impairment preventing informed consent or study compliance
Renal/General Medical Exclusions:
-
End-stage kidney disease (ESKD) on maintenance hemodialysis or peritoneal dialysis
-
Pregnancy or breastfeeding
-
Active malignancy (except non-melanoma skin cancer)
-
Severe hepatic disease (Child-Pugh Class C cirrhosis)
-
Immunosuppression (within 8 weeks of enrollment) or active immunosuppressive therapy
Skin/Electrode-Related Exclusions:
-
Active infection or severe lesions at tragus preventing electrode placement
-
Known allergy to gold or electrode materials
-
Implanted device at <2 cm proximity to ear tragus (e.g., cochlear implant, cerebral shunt, invasive Vagus Nerve Stimulation (VNS))
Substance Use/Other:
-
Active substance uses disorder (within 1 year) or alcohol use >14 drinks/week
-
Participation in another clinical trial within 30 days
-
Any condition that, in the investigator's judgment, would make participation unsafe or preclude compliance
-
Prisoners
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:阶乘赋值
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
假比较器:Sham-AM
Participants will use the sham-device for 1 hr/day at 7:00 AM. |
The device is equipped with a "ramp-down sham mode". In this mode, no electrical stimulation will occur for the remainder of the session and participant intensity adjustments are disabled. Participants will use the sham-device at home once daily for 60 minutes either in the morning at 7am or in the evening at 7pm. |
|
假比较器:Sham-PM
Participants will use the sham-device for 1 hr/day at 7:00 PM. |
The device is equipped with a "ramp-down sham mode". In this mode, no electrical stimulation will occur for the remainder of the session and participant intensity adjustments are disabled. Participants will use the sham-device at home once daily for 60 minutes either in the morning at 7am or in the evening at 7pm. |
|
实验性的:Active-AM
Participants will use the active AVNT device for 1 hr/day at 7:00 AM. |
The device consists of a handheld stimulation unit (~2 inches) connected to a tragus earpiece electrode (worn like an in-ear headphone, removed after each session). Participants will undergo AVNT™ at home once daily for 60 minutes either in the morning at 7am or in the evening at 7pm at a pulse width of 250 μs, frequency of 20 Hz, and comfortable, patient-titrated intensity based on personalized perceptual thresholds.
其他名称:
|
|
实验性的:Active-PM
Participants will use the active AVNT device for 1 hr/day at 7:00 PM. |
The device consists of a handheld stimulation unit (~2 inches) connected to a tragus earpiece electrode (worn like an in-ear headphone, removed after each session). Participants will undergo AVNT™ at home once daily for 60 minutes either in the morning at 7am or in the evening at 7pm at a pulse width of 250 μs, frequency of 20 Hz, and comfortable, patient-titrated intensity based on personalized perceptual thresholds.
其他名称:
|
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 |
|---|---|---|
|
Change in Orthostatic Heart Rate Response
大体时间:Week 0, Week 2
|
Difference in standing heart rate at 1 minute minus baseline seated heart rate, averaged across daily home measurements in Week 0 (baseline) and last 3-5 days of Week 2 (post-intervention). |
Week 0, Week 2
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change in high-sensitivity C-reactive protein (hs-CRP) (pg/mL)
大体时间:Week 0, Week 2
|
Week 0, Week 2
|
|
|
Change in Interleukin-6 (IL-6) (pg/mL)
大体时间:Week 0, Week 2
|
Week 0, Week 2
|
|
|
Change in Urine Albumin-Creatinine Ratio (UACR) (mg/g creatinine)
大体时间:Week 0, Week 2
|
Week 0, Week 2
|
|
|
Change in Composite Autonomic Symptom Score-31 (COMPASS-31)
大体时间:Week 0, Week 2
|
The COMPASS-31 is a 31-item, self-administered clinical questionnaire used to measure the severity and distribution of autonomic nervous system symptoms (dysautonomia). Scores range from 0 to 100, where higher scores indicate worse autonomic dysfunction. |
Week 0, Week 2
|
|
Percentage of participants who achieved ≥85% prescribed minutes (714 of 840 min)
大体时间:Week 2
|
Week 2
|
|
|
Percentage of patients that completed ≥70% of scheduled autonomic measurements
大体时间:Week 2
|
Week 2
|
合作者和调查者
调查人员
- 首席研究员:Qandeel Soomro, MD, MS、NYU Langone Health
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
其他相关的 MeSH 术语
其他研究编号
- 26-00938
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
The de-identified participant data from the final research dataset will be shared upon reasonable request beginning 9 to 36 months after publication or as required by a condition of awards or supporting agreements, provided the requesting investigator executes a data use agreement with NYU Langone Health. This instance of data sharing will also require separate IRB review as well as review from NYU Langone's Data Sharing Strategy Board (DSSB). Requests should be directed to: Qandeel.Soomro@nyulangone.org. The protocol and statistical analysis plan will be posted on Clinicaltrials.gov only as required by federal regulation or supporting awards and agreements.
IPD 共享时间框架
Beginning 9 months and ending 36 months following article publication or as required by a condition of awards and agreements supporting the research.
IPD 共享访问标准
The investigator who proposed to use the data will be granted access upon reasonable request. Requests should be directed to Qandeel.Soomro@nyulangone.org. To gain access, data requestors will need to sign a data access agreement. This instance of data sharing will also require separate IRB review as well as review from NYU Langone's DSSB.
IPD 共享支持信息类型
- 研究方案
- 树液
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.