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.
調査の概要
状態
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Qandeel Soomro, MD, MS
- 電話番号:929-573-1168
- メール:Qandeel.Soomro@nyulangone.org
研究連絡先のバックアップ
- 名前:David Moran
- 電話番号:212-263-4072
- メール:David.Moran@nyulangone.org
研究場所
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New York
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New York、New York、アメリカ、10016
- NYU Langone Health
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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:
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Implantable cardioverter-defibrillator (ICD) or other implanted cardiac device
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Known severe coronary disease (≥70% stenosis in major vessel) or myocardial infarction within past 5 years
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Hospitalized within 4 weeks
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Syncope or unexplained loss of consciousness within past 12 months
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Uncontrolled arrhythmia (atrial fibrillation with resting heart rate >110 bpm, recent runs of sustained ventricular tachycardia or supraventricular tachycardia) within 3 months.
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Severe bradycardia (<40 bpm at rest, symptomatic) , or second- or third-degree atrioventricular (AV) block without a functioning pacemaker
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Neurological/Anatomical Exclusions:
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History of vagotomy (surgical cutting of vagus nerve)
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Trigeminal neuralgia within 1 year
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Epilepsy or seizure disorder (unless well-controlled defined as seizure free with stable dose of medication for ≥2 years)
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Dementia or cognitive impairment preventing informed consent or study compliance
Renal/General Medical Exclusions:
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End-stage kidney disease (ESKD) on maintenance hemodialysis or peritoneal dialysis
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Pregnancy or breastfeeding
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Active malignancy (except non-melanoma skin cancer)
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Severe hepatic disease (Child-Pugh Class C cirrhosis)
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Immunosuppression (within 8 weeks of enrollment) or active immunosuppressive therapy
Skin/Electrode-Related Exclusions:
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Active infection or severe lesions at tragus preventing electrode placement
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Known allergy to gold or electrode materials
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Implanted device at <2 cm proximity to ear tragus (e.g., cochlear implant, cerebral shunt, invasive Vagus Nerve Stimulation (VNS))
Substance Use/Other:
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Active substance uses disorder (within 1 year) or alcohol use >14 drinks/week
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Participation in another clinical trial within 30 days
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Any condition that, in the investigator's judgment, would make participation unsafe or preclude compliance
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Prisoners
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:ランダム化
- 介入モデル:階乗代入
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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偽コンパレータ: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. |
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偽コンパレータ: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. |
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実験的: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.
他の名前:
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実験的: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.
他の名前:
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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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Change in Orthostatic Heart Rate Response
時間枠:Week 0, Week 2
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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
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Change in high-sensitivity C-reactive protein (hs-CRP) (pg/mL)
時間枠:Week 0, Week 2
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Week 0, Week 2
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Change in Interleukin-6 (IL-6) (pg/mL)
時間枠:Week 0, Week 2
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Week 0, Week 2
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Change in Urine Albumin-Creatinine Ratio (UACR) (mg/g creatinine)
時間枠:Week 0, Week 2
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Week 0, Week 2
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Change in Composite Autonomic Symptom Score-31 (COMPASS-31)
時間枠:Week 0, Week 2
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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
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Percentage of participants who achieved ≥85% prescribed minutes (714 of 840 min)
時間枠:Week 2
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Week 2
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Percentage of patients that completed ≥70% of scheduled autonomic measurements
時間枠:Week 2
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Week 2
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協力者と研究者
スポンサー
捜査官
- 主任研究者:Qandeel Soomro, MD, MS、NYU Langone Health
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
追加の関連 MeSH 用語
その他の研究ID番号
- 26-00938
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
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 共有時間枠
Beginning 9 months and ending 36 months following article publication or as required by a condition of awards and agreements supporting the research.
IPD 共有アクセス基準
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 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
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。
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。