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CTRI Number  CTRI/2024/12/078441 [Registered on: 23/12/2024] Trial Registered Prospectively
Last Modified On: 20/12/2024
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Medical Device
Physiotherapy (Not Including YOGA) 
Study Design  Randomized, Parallel Group, Placebo Controlled Trial 
Public Title of Study   Transcutaneous Electrical Stimulation of Vagus Nerve Among Stroke survivors 
Scientific Title of Study   Efficacy and safety of Transcutaneous Electrical Stimulation of Vagus Nerve in Upper Limb Motor Recovery Among Stroke survivors: A Randomized Controlled Trial 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Sandip Dhole 
Designation  Associate Professor 
Affiliation  AIIMS, Bibinagar 
Address  PMR Department AIIMS, Bibinagar (Hyderabad Metropolitan Region) Bibinagar, Dist.Yadadari Bhuvanagiri, Telangana-508126
AIIMS, Bibinagar (Hyderabad Metropolitan Region) Bibinagar, Dist.Yadadari Bhuvanagiri, Telangana-508126
Nalgonda
TELANGANA
508126
India 
Phone  9867927350  
Fax    
Email  drsandipdhole@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Sandip Dhole 
Designation  Associate Professor 
Affiliation  AIIMS, Bibinagar 
Address  PMR Department AIIMS, Bibinagar (Hyderabad Metropolitan Region) Bibinagar, Dist.Yadadari Bhuvanagiri, Telangana-508126
AIIMS, Bibinagar (Hyderabad Metropolitan Region) Bibinagar, Dist.Yadadari Bhuvanagiri, Telangana-508126

TELANGANA
508126
India 
Phone  9867927350  
Fax    
Email  drsandipdhole@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Sandip Dhole 
Designation  Associate Professor 
Affiliation  AIIMS, Bibinagar 
Address  PMR Department AIIMS, Bibinagar (Hyderabad Metropolitan Region) Bibinagar, Dist.Yadadari Bhuvanagiri, Telangana-508126
AIIMS, Bibinagar (Hyderabad Metropolitan Region) Bibinagar, Dist.Yadadari Bhuvanagiri, Telangana-508126
Nalgonda
TELANGANA
508126
India 
Phone  9867927350  
Fax    
Email  drsandipdhole@gmail.com  
 
Source of Monetary or Material Support  
AIIMS, Bibinagar (Hyderabad Metropolitan Region) Bibinagar, Dist.Yadadari Bhuvanagiri, Telangana-508126 
 
Primary Sponsor  
Name  NA 
Address  NA 
Type of Sponsor  Other [NA] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
DR SANDIP DHOLE  AIIMS, Bibinagar  AIIMS, Bibinagar (Hyderabad Metropolitan Region) Bibinagar, Dist.Yadadari Bhuvanagiri, Telangana-508126
Nalgonda
TELANGANA 
09867927350

drsandipdhole@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
AIIMS BBN Ethical Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: G811||Spastic hemiplegia,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  sham stimulation with the clip electrodes placed at Cymba conchae at the left ear for 30 minutes, once a day, six days per week for 3 weeks followed by rehabilitation therapy only 3week course of 2h therapy sessions, 3x week at least 300 to 400 movements per session.   Group B will get sham stimulation with the clip electrodes placed at Cymba conchae at the left ear for 30 minutes, once a day, six days per week for 3 weeks followed by rehabilitation therapy only 3week course of 2h therapy sessions, 3x week at least 300 to 400 movements per session.  
Intervention  Vagus nerve stimulation using TENS   The Group A will get Vagus nerve stimulation using TENS with the clip electrodes placed at the Cymba conchae at the left ear 0.3ms pulses, 30Hz, intensity maximum tolerable level for 30 minutes, once a day six days per week for 3 weeks with continuous monitoring of vital parameter in presence of a senior physiotherapist and emergency medical care and also underwent rehabilitation therapy only 3 week course of h therapy sessions, 3x week, at least 300 to 400 movements per session.  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  80.00 Year(s)
Gender  Both 
Details  1.Age: 18 years and above.
2.Patients having an ischemic stroke for at least 3 months previously
3.No strict cut-offs will be required for baseline upper limb function as long as the
4.Participant could engage with the therapist and perform the limb movements.
 
 
ExclusionCriteria 
Details  1.Patients having impairments of upper limb function other than those caused by stroke
2.Hemorrhagic Stroke
3.Patients having aphasia or cognitive difficulties severe enough to interfere with the informed consent process, task specific practice or communication of adverse events,
4.Pregnant or trying to get pregnant patients
5.Patients having a pacemaker or other implanted electrical device
6.Patients having severe spasticity (a Modified Ashworth Score12 ≥3).
7.Low hearth rate (<60 bpm);
8.Apraxia
9.Excessive pain in any joint of the paretic extremity
10.Advanced liver, kidney, cardiac, or pulmonary disease
11.History of significant alcohol or drug abuse
12.Depression or use of neuropsychotropic drugs such as antidepressants or benzodiazepines

 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   An Open list of random numbers 
Blinding/Masking   Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
Demographics, time since stroke, medication and vascular risk factors will be obtained from participants. Hospital records and imaging results will be viewed to record the size, location and precise date of the stroke.
Two measures of upper limb movement and functional independence will be assessed:
1. Upper Limb Fugl-Meyer (UFM)
2. Action Recovery Arm Test (ARAT).
 
These assessments will be performed at baseline and at the end of the intervention (3
weeks). To observe long-term effects, evaluation will be done at 6 weeks and 12 weeks after
first intervention. 
 
Secondary Outcome  
Outcome  TimePoints 
NA  NA 
 
Target Sample Size   Total Sample Size="30"
Sample Size from India="30" 
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   Phase 3 
Date of First Enrollment (India)   01/01/2025 
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="1"
Months="1"
Days="1" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
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  

Stroke is a neurological condition caused by vascular problems such as cerebral infarction and/or intra cerebral or subarachnoid hemorrhage1. Motor impairment occurs in 85% of patients with stroke, and it is considered one of the main problems resulting from this condition.

Efforts have been made to develop therapies that can improve motor impairment in stroke patients 8 Among these therapies are: constraint-induced movement 9, mirror therapy 10 and resistance training 11, however, these interventions have a low level of adherence 12 and the evidence supporting their effects is still weak 9-11

Recently, Vagus Nerve Stimulation (VNS) has been proposed as an intervention that could have beneficial effects in the recovery of motor function in these patients, since it contributes to the generation of adaptive neuroplasticity and the activation of neuromodulators that reduce brain inflammation 13, 14

Objective of our study to study the efficacy and safety of Transcutaneous Electrical Stimulation of Vagus Nerve in Upper Limb Motor Recovery among Stroke survivors.

We are going to do prospective randomized study on stroke patients having upper limb motor impairment.

The subject will comprise of clinically diagnosed stroke patients in OPD and IPD at AIIMS Bibinagar, Hospital, fulfilling the inclusion criteria of the study. In this study we are going to enroll patients by stratified randomization in two groups 30 in each group.

The Group A will get Vagus nerve stimulation using TENS with the clip electrodes placed at the Cymba conchae at the left ear (0.3ms pulses, 30Hz, intensity = maximum tolerable level) for 30 minutes, once a day, six days per week for 3 weeks with continuous monitoring of vital parameter in presence of a senior physiotherapist and emergency medical care and also underwent rehabilitation therapy only (3-week course of 2-h therapy sessions, 3x week, at least 300 to 400 movements per session).

Group B will get sham stimulation with the clip electrodes placed at Cymba conchae at the left ear for 30 minutes, once a day, six days per week for 3 weeks followed by rehabilitation therapy only (3-week course of 2-h therapy sessions, 3x week, at least 300 to 400 movements per session).

Outcome will be measured after 3 weeks of treatment by Upper Limb Fugl-Meyer (UFM) and Action Recovery Arm Test. To observe long-term effects, evaluation will be done at 6 weeks and 12 weeks after first intervention.

The main safety outcome measure will be the number of serious adverse events related to the device or therapy, such as skin toxicity (pain, skin erythema, burns, etc.), hoarseness, and dysphasia. Heart rate (HR) and blood pressure (BP) will also observe before and after each intervention.

Outcome Assessor will be blinded to study group allocation.

We are going to compare the results of these two groups to see efficacy and safety of vagus nerve stimulation in stroke patients of upper limb motor recovery.

 
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