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CTRI Number  CTRI/2025/11/098233 [Registered on: 28/11/2025] Trial Registered Prospectively
Last Modified On: 27/11/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Medical Device 
Study Design  Single Arm Study 
Public Title of Study   A Multicenter study to check how well Nerve Vue can detect Peripheral Arterial Disease (PAD) 
Scientific Title of Study   A Prospective, Multicenter clinical trial to validate the diagnostic accuracy of Nerve Vue in detecting Peripheral Arterial Disease (PAD) 
Trial Acronym  NERVE-PAD 
Secondary IDs if Any  
Secondary ID  Identifier 
NV-2025-01 Version 1.0 26 Mar 2025  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Gayathri Choda 
Designation  Founder & CEO 
Affiliation  Aarca Research India Pvt, Ltd 
Address  41/21-1, 29th Cross, 7th Block Department of Vascular Surgery, room number 101, Ground Floor Jayanagar.

Bangalore
KARNATAKA
560082
India 
Phone  9963522288  
Fax    
Email  gchoda@aarcaresearch.com  
 
Details of Contact Person
Scientific Query
 
Name  Gayathri Choda 
Designation  Founder & CEO 
Affiliation  Aarca Research India Pvt, Ltd 
Address  41/21-1, 29th Cross, 7th Block Department of Vascular Surgery, room number 101 Ground Floor Jayanagar.

Bangalore
KARNATAKA
560082
India 
Phone  9963522288  
Fax    
Email  gchoda@aarcaresearch.com  
 
Details of Contact Person
Public Query
 
Name  Gayathri Choda 
Designation  Founder & CEO 
Affiliation  Aarca Research India Pvt, Ltd 
Address  41/21-1, 29th Cross, 7th Block Department of Vascular Surgery, room number 101, Ground Floor Jayanagar.

Bangalore
KARNATAKA
560082
India 
Phone  9963522288  
Fax    
Email  gchoda@aarcaresearch.com  
 
Source of Monetary or Material Support  
Aarca Research India Pvt. Ltd 41/21-1, 29th Cross, 7th Block Jayanagar BENGALURU, KARNATAKA 560082 India 
 
Primary Sponsor  
Name  Aarca Research India Pvt. Ltd 
Address  41/21-1, 29th Cross, 7th Block Jayanagar BENGALURU, KARNATAKA 560082 India 
Type of Sponsor  Other [Medical device manufacturing] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 2  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
DrJ Sai Rakesh  Aarca Research  Room 76,4th floor, Dept of clinical research, Sanskriti Signet, outer ring road,stage 2, BTM layout 2nd Stage, Bengaluru, Karnataka, India 560068
Bangalore
KARNATAKA 
9963522288

contact@aarcaresearch.com 
Dr Anuhya choda  Medstar Speciality Hospital  Department of Clinical Research #641/17/1/3, kodigehalli, Main Road, Sahakarnagr Bangalore 560092, Karnataka, India
Bangalore
KARNATAKA 
9177022298

achoda@aarcaresearch.com 
 
Details of Ethics Committee  
No of Ethics Committees= 2  
Name of Committee  Approval Status 
ACE Independent Ethics Committee  Approved 
ACE Independent Ethics Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Approved/Obtained 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  detect and monitor Peripheral Arterial Disease (PAD) in human subjects. 
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  NerveVue  NerveVue is a non-invasive, multi-sensor diagnostic device designed to assess peripheral arterial health by measuring hemodynamic and arterial pressure waveform parameters. Each participant will undergo one session using NerveVue for vascular data recording. No drug or therapeutic intervention is involved. 
Comparator Agent  Standard Ankle-Branchial Index (ABI) measurement  Doppler-based Ankle-Branchial Index (ABI) measurement used as standard reference method for peripheral arterial assessment 
 
Inclusion Criteria  
Age From  25.00 Year(s)
Age To  34.00 Year(s)
Gender  Both 
Details  Age greater than or equal to 35 years.
or
Age 25 to 34 years with one or more of the following risk factors:
- BMI greater than 25 kg/m²
- Elevated waist circumference: greater than 35 inches for women and greater than 40 inches for men
- Habitually physically inactive (does not exercise regularly)
- Has a first-degree relative with diabetes
- Ethnicity with elevated risk for type 2 diabetes
- Has delivered a baby weighing greater than 9 lb or was diagnosed with gestational diabetes
- Hypertension (greater than or equal to 130/greater than or equal to 85 mmHg) or being treated for hypertension
- HDL cholesterol level less than 35 mg/dL and/or a fasting triglyceride level greater than or equal to 250 mg/dL (or being treated for Dyslipidemia with medication)
- Previously diagnosed with Polycystic Ovary Syndrome (PCOS)
- Had impaired glucose tolerance or impaired fasting glucose on previous testing within the last three years
- Conditions associated with insulin resistance, such as acanthosis nigricans
- History of vascular disease including heart attack, stroke, angina, coronary heart disease, atherosclerosis, congestive heart failure, or
peripheral arterial disease
 
 
ExclusionCriteria 
Details  Age under 25 years
or
- Received investigational treatments in the past 14 days.
- Presence of psychosocial issues that interfere with the ability to follow study procedures.
- conditions that causes secondary diabetes including cushing syndrome, acromegaly, hemochromatosis, Pancreatitis, or cystic fibrosis
- Diagnosed with any type of diabetes, including type 1 or type 2
- Taking glucose-lowering medications with the exception of metformin.
- Known to be pregnant
- Receiving dialysis or having known renal compromise.
- Scars, tattoos, rashes, or other disruptions/discolorations on the limbs or areas of sensor application that may interfere with proper usage of NerveVue.
- Recent (within the past month) or current oral steroid therapy or chemotherapy, or chemotherapy within the past 12 months.
- Receiving medications that fluoresce or known to have, or be at risk for, photosensitivity reactions (e.g., sensitive to ultraviolet light, or taking medication known to cause photosensitivity).


 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Diagnostic Accuracy of NerveVue: The primary objective is to evaluate
NerveVue’s sensitivity and specificity in detecting early or subclinical Peripheral
Arterial Disease (PAD). This includes comparing the device’s measurement
outputs (e.g., pulse-wave indices, perfusion metrics) against established diagnostic
standards, such as the Ankle-Brachial Index (ABI) and Doppler Ultrasound. 
There is only one visit, i,e Baseline /screening /Enrolment visit 
 
Secondary Outcome  
Outcome  TimePoints 
- Comparison with Standard Diagnostic Methods: A comparative analysis will be performed to assess the level of agreement between NerveVue results & existing PAD assessment techniques. Concordance, correlation coefficients, & potential advantages or limitations in various clinical environments will be documented.
- Usability & Acceptability: The study will collect structured feedback from both participants & clinical personnel on factors such as ease of use, comfort, setup time, & overall user satisfaction. These insights will inform potential device refinements & practical considerations for routine clinical use.
- Clinical Correlations: Data obtained through NerveVue will be examined in relation to other clinical or metabolic markers, such as patient-reported symptoms, comorbid conditions (e.g., diabetes), & broader cardiovascular risk profiles.
- Feasibility of early detection- determine
- Longitudinal Monitoring 
There is one visit, i,e Baseline /screening/Enrolment visit 
 
Target Sample Size   Total Sample Size="500"
Sample Size from India="500" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   29/12/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="0"
Months="2"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

The main purpose of this study is to evaluate whether Nerve Vue can accurately detect and monitor Peripheral Arterial Disease (PAD) in human subjects. Specifically, the study aims to determine if the device can identify early signs of compromised blood flow that are characteristic of PAD, thereby enabling proactive healthcare interventions and personalized care for at-risk individuals.

Background

Cardiovascular and metabolic health disorders remain major global health concerns, contributing to significant morbidity, mortality, and healthcare costs. Among these disorders, Peripheral Arterial Disease (PAD) is a particularly prevalent condition characterized by reduced blood flow to the limbs due to arterial narrowing or blockages. PAD often coexists with metabolic syndrome-an umbrella term encompassing risk factors such as obesity, insulin resistance, dyslipidaemia, and hypertension. When left unaddressed, PAD can lead to serious complications such as pain, limited mobility, and increased risk of cardiovascular events. Despite its prevalence, early detection of PAD remains challenging. Conventional diagnostic methods (e.g. Ankle-Brachial Index, Doppler ultrasound) are effective but can be time-intensive or require specialized equipment and expertise. This often results in underdiagnosis of PAD- especially among individuals with subclinical or mild disease. Consequently, there is a need for non-invasive, user-friendly technologies that enable earlier identification and monitoring of vascular compromise in diverse healthcare settings. In line with this need, the investigational device Nerve Vue integrates photoplethysmography (PPG) and piezoelectric sensors to capture and analyse peripheral pulse signals. By providing a rapid and comprehensive assessment of blood flow, Nerve Vue may allow healthcare professionals to identify early vascular changes indicative of PAD. This could ultimately facilitate proactive management strategies, mitigate progression, and improve overall vascular outcomes in affected individuals.

 
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