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CTRI Number  CTRI/2024/11/077071 [Registered on: 19/11/2024] Trial Registered Prospectively
Last Modified On: 28/08/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug
Ayurveda 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   A study on Ayurvedic management of Sensory neural hearing loss with Asanabilwadi taila karnapoorana,Nasya with Ksheerabala taila 101 avarthi and Narasimha choorna orally 
Scientific Title of Study   Evaluation of the efficacy of Asanabilwadi taila Karnapoorana, Nasya with Ksheerabala taila 101 avarthi and Narasimha choorna orally in Badhirya- Sensory neural hearing loss- an open-label double arm randomized controlled clinical 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 Harshitha B Dev 
Designation  MS Scholar 
Affiliation  All India Institute of Ayurveda 
Address  Room no-505 Department of shalakyatantra 5th floor Academic block All India Institute of Ayurveda Gautampuri Sarita vihar New Delhi 110076

South
DELHI
110076
India 
Phone  9447626735  
Fax    
Email  harshithabdev@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Narayan Bavalatti 
Designation  Additional Professor 
Affiliation  All India Institute of Ayurveda 
Address  Room no-509 Department of shalakyatantra 5th floor Academic block All India Institute of Ayurveda Gautampuri Sarita vihar New Delhi 110076

South
DELHI
110076
India 
Phone  9650715615  
Fax    
Email  eyenimi@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Harshitha B Dev 
Designation  MS Scholar 
Affiliation  All India Institute of Ayurveda 
Address  Room no 505 Department of Shalakyatantra 5th floor Academic block All India Institute of Ayurveda Goutampuri Sarita vihar New Delhi 110076

South
DELHI
110076
India 
Phone  9447626735  
Fax    
Email  harshithabdev@gmail.com  
 
Source of Monetary or Material Support  
All India Institute of Ayurveda New Delhi 
 
Primary Sponsor  
Name  All India Institute of Ayurveda 
Address  All India Institute of Ayurveda Gautampuri Sarita vihar New Delhi 110076 
Type of Sponsor  Government medical college 
 
Details of Secondary Sponsor  
Name  Address 
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 Harshitha B Dev  All India Institute of Ayurveda,New Delhi  Room no-509 Department of shalakyatantra 5th floor Academic block All India Institute of Ayurveda Gautampuri Sarita vihar New Delhi 110076
South
DELHI 
9447626735

harshithabdev@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committe,All India Institute of Ayurveda  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition:H838||Other specified diseases of innerear. Ayurveda Condition: BADHIRYAM,  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmDrugClassical(1) Medicine Name: Narasimha choorna, Reference: Bhaishajyaratnavali, Route: Oral, Dosage Form: Churna/ Powder, Dose: 6(g), Frequency: bd, Bhaishajya Kal: Adhobhakta, Duration: 45 Days, anupAna/sahapAna: Yes(details: -Unequal quantities of Ghrita and Madhu), Additional Information: -
2Comparator ArmDrugClassical(1) Medicine Name: Sarivadi vati, Reference: Bhaishajyaratnavali, Route: Oral, Dosage Form: Gutika/Vati/Ghana Vati/ Tablets, Dose: 500(mg), Frequency: bd, Bhaishajya Kal: Adhobhakta, Duration: 45 Days, anupAna/sahapAna: Yes(details: -Lukewarm water), Additional Information: -
3Intervention ArmProcedure-karNapUraNam, कर्णपूरणम् (Procedure Reference: Ashtangahridayam, Procedure details: Karnapoorana will be done with Asanabilwadi taila in a dose of 1 ml per ear for a duration of 3 sitting of 7 days with 7 days gap)
(1) Medicine Name: Asanabilwadi taila, Reference: Sahasrayogam, Route: Otic, Dosage Form: Taila, Dose: 1(ml), Frequency: od, Duration: 21 Days
4Intervention ArmProcedure-marSaH, मर्श (Procedure Reference: Ashtangahridayam, Procedure details: Nasya will be done with Ksheerabala taila 101 avarthi in a dose of 6 drops in each nostrills for a duration of 3 sitting of 7 days with 7 days gap)
(1) Medicine Name: Ksheerabala taila 101 avarthi, Reference: Ashtangahridayam, Route: Nasal, Dosage Form: Bindu/ Drops/ Spray (Karna/ Nasa/ Netra/ Mukha), Dose: 6(drops), Frequency: od, Duration: 21 Days
5Comparator ArmProcedure-marSaH, मर्श (Procedure Reference: Ashtangahridayam, Procedure details: Nasya will be done with Shadbindu taila in a dose of 6 drops in each nostrills for a duration of 3 sitting of 7 days with 7 days gap)
(1) Medicine Name: Shadbindu taila, Reference: Bhaishajyaratnavali, Route: Nasal, Dosage Form: Bindu/ Drops/ Spray (Karna/ Nasa/ Netra/ Mukha), Dose: 6(drops), Frequency: od, Duration: 21 Days
6Comparator ArmProcedure-karNapUraNam, कर्णपूरणम् (Procedure Reference: Ashtangahridayam, Procedure details: Karnapoorana will be done with Bilwadi taila in a dose of 1 ml per ear for a duration of 3 sitting of 7 days with 7 days gap)
(1) Medicine Name: Bilwadi taila, Reference: Susruta samhita, Route: Otic, Dosage Form: Taila, Dose: 1(ml), Frequency: od, Duration: 21 Days
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  INCLUSION CRITERIA

1. Patients having signs and symptoms of Badhirya (SNHL) with mild (26-40 dB) to moderate (41-60 dB) hearing loss will be selected.
2. Patients of either sex aged between 18 to 60 years.
3. The patient is willing and able to participate in the study.
4. Patients fit for Nasya Karma.
5. Patients fit for Karnapoorana karma.
6. Patients with intact tympanic membrane.
 
 
ExclusionCriteria 
Details  1. Conductive and mixed hearing loss
2. Subjects associated with tympanic membrane perforation.
3. Patients with a degree of hearing impairment more than 61 dB.
4. Patients with otorrhoea.
5. Pregnant women
6. Patients with congenital hearing loss.
7. Patients who require otological surgical intervention.
8. Malignancy related to the external middle and internal ear.
9. Patients with systemic illnesses like DM Hypertension Tuberculosis.
10.Patients who are using hearing aid.
 
 
Method of Generating Random Sequence   Permuted block randomization, variable 
Method of Concealment   Other 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
Improvement of air conduction thresholds in patients presenting with hearing loss in the range of 26 to 60 dB based on pure tone average.  Assessment will be done before treatment,15th day,30th day and 45th day of the trial. 
 
Secondary Outcome  
Outcome  TimePoints 
1. Improvement in associated symptoms of Badhirya (SNHL) like Karnanada (Tinnitus)and Bhrama(Giddiness)
2. The study will provide physicochemical and organoleptic properties of Asanabilwadi taila Ksheerabala taila 101 Avarthi and Narasimha Choorna.
 
Assessment will be before treatment,15th day,30th day and 45th day of the trial. 
 
Target Sample Size   Total Sample Size="40"
Sample Size from India="40" 
Final Enrollment numbers achieved (Total)= "0"
Final Enrollment numbers achieved (India)="40" 
Phase of Trial   Phase 2 
Date of First Enrollment (India)   01/01/2025 
Date of Study Completion (India) 29/05/2026 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="0"
Months="1"
Days="15" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details
Modification(s)  
N/A 
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary  

Title: Evaluation of the efficacy of Asanabilwadi taila Karnapoorana, Nasya with Ksheerabala taila 101 avarthi and Narasimha choorna orally in Badhirya- Sensory neural hearing loss- an open-label double arm randomized controlled clinical trial.


RESEARCH QUESTION

 What is the efficacy of Asanabilwadi Taila Karnapoorana,  Nasya with Ksheerabala Taila 101 Avarthi and Narasimha Choorna orally compared with that of Bilwadi Taila Karnapoorana,  Nasya with Shadbindu Taila and Sarivadi vati orally for a duration of 45 days in the management of Badhirya - Sensory Neural Hearing Loss?

NULL HYPOTHESIS (Ho)

 There is no significant difference between the efficacy of Asanabilwadi Taila Karnapoorana (1 ml in each ear at morning), Nasya with Ksheerabala Taila 101 Avarthi (6 drops in each nostril) and Narasimha Choorna (6 g twice daily) orally in comparison to Bilwadi Taila Karnapoorana (1 ml-at morning), Nasya with Shadbindu Taila (6 drops in each nostril) and Sarivadi vati (2 tablets (250 mg) twice daily) orally for a duration of 45 days in Badhirya (sensory neural hearing loss).

ALTERNATE HYPOTHESIS(H1)

 There is a significant difference between the efficacy of Asanabilwadi Taila Karnapoorana (1 ml in each ear at morning),  Nasya with Ksheerabala Taila 101 Avarthi (6 drops in each nostril), and Narasimha choorna (6 g twice daily) orally in comparison to Bilwadi Taila Karnapoorana (1 ml-at morning), Nasya with Shadbindu Taila (6 drops in each nostril) and Sarivadi vati (2 tablets (250 mg) twice daily) orally for a duration of 45 days in Badhirya (sensory neural hearing loss).

Need of the study

A complete or partial loss of hearing in one or both ears is referred to as hearing impairment. Its clinical characteristics are quite similar to those of Badhirya as described in Ayurveda, and it may be congenital or acquired. Three forms of hearing loss are recognized in clinical practice: sensory neural, conductive, and mixed. Conductive hearing loss (CHL) is the term used to describe hearing loss that results from sound conduction from the external ear to the stapediovestibular joint. Sensory neural hearing loss (SNHL) is caused by disorders of the cochlea, vestibulocochlear nerve, and its central connections. Both the conductive hearing loss and sensory neural hearing loss elements are present in mixed hearing loss. Assistive devices, implants, and hearing aids are the most often utilized equipment in the rehabilitation of hearing impairment. However, using these gadgets may be challenging as their users’ perception of sounds is limited compared to individuals with normal hearing. In more severe circumstances where standard hearing aids offer little benefit, a cochlear implant may be an option. The Ayurvedic treatment for hearing impairment can be an alternative to conventional care because the treatment offered by the conventional system of medicine is more expensive and out of the grasp of the average Indian people. So the current study aims at exploring a cost-effective and safe remedy through Ayurvedic treatment for the management of hearing impairment. Therefore, it is required to find effective treatment measures for the disease.

These factors have been taken into consideration when choosing the study topic for this illness. 

AIM
To evaluate the efficacy of Karnapoorana with Asanabilwadi taila, Nasya with Ksheerabala taila 101 Avarthi along with Narasimha choorna orally in the management of Badhirya (sensory neural hearing loss) in comparison with Bilwadi taila Karnapoorana, Nasya with Shadbindu Taila and Sarivadi Vati orally for a duration of 45 days.

 PRIMARY OBJECTIVE

  • To evaluate the efficacy of Asanabilwadi Taila Karnapoorana, Nasya with Ksheerabala Taila 101 Avarthi and Narasimha Choorna orally in improving the air conduction thresholds in patients presenting with hearing loss in the range of 26-60 dB based on pure tone average.

 SECONDARY OBJECTIVES

  •      To evaluate the efficacy of Asanabilwadi Taila Karnapoorana, Nasya with Ksheerabala Taila 101 Avarthi and Narasimha Choorna orally in associated symptoms of  Badhirya like, Karnanada (Tinnitus) and Bhrama (giddiness).
  •       To evaluate the physicochemical and organoleptic properties of Asanabilwadi taila, Ksheerabala taila 101 Avarthi, and Narasimha Choorna.

TYPE OF STUDY DESIGN

Open labelled double arm randomized controlled clinical trial

Group 1- Intervention with Asanabilwadi taila Karnapoorana, Nasya with Ksheerabala  Taila 101 Avarthi, and Narasimha choorna orally.

Group 2- Control with Bilwadi taila Karnapoorana, Nasya with Shadbindu Taila, and Sarivadi Vati orally

STUDY SETTING:

Department of Shalakya Tantra of AIIA, Sarita Vihar, New Delhi

STUDY POPULATION:

Patients attending the OPD and IPD of the department of Shalakya Tantra, and those referred from other departments of All India Institute of Ayurveda, New Delhi, shall be selected irrespective of gender, religion, race, occupation, etc. based on the diagnostic, selection criteria and be enrolled in the study.

Sample size - 20 in each group

INCLUSION CRITERIA

 1. Patients having signs and symptoms of Badhirya (SNHL) with mild (26-40 dB) to moderate  (41-60 dB) hearing loss will be selected.

2. Patients of either sex aged between 18 to 60 years.

3. The patient is willing and able to participate in the study.

4. Patients fit for Nasya Karma.

5. Patients fit for Karnapoorana karma.

6. Patients with intact tympanic membrane.

EXCLUSION CRITERIA

 1. Conductive & mixed hearing loss

 2. Subjects associated with tympanic membrane perforation.

 3. Patients with a degree of hearing impairment (>61 dB).

 4. Patients with otorrhoea.

 5. Pregnant women

 6. Patients with congenital hearing loss.

 7. Patients who require otological surgical intervention.

 8. Malignancy related to the external, middle, and internal ear.

 9. Patients with systemic illnesses like DM, Hypertension, Tuberculosis…etc.

10.Patients who are using hearing aid.

ASSESSMENT CRITERIA-

Diagnosis will be made according to the Ayurveda and modern subjective and objective parameters.

Subjective Parameters

1. Badhirya – Hearing impairment

2. Karnanada-Tinnitus

3. Bhrama- Vertigo

Objective Parameters

1. Tuning fork tests

2. Otoscopy

3. Pure tone Audiometry

4. Tympanometry

These tests are performed to rule out cases of Badhirya (SNHL).

Routine ear examinations will be carried out before and after treatment.

DIAGNOSTIC CRITERIA

Badhirya (SNHL) will be assessed by using the WHO hearing loss grading scale based on Pure Tone Audiometry.

 WHO hearing loss grading scale[25]

Grade of impairment

Corresponding audiometric ISO value

Performance

0: no impairment

25 dB or better

No or very slight hearing problems. Able to hear whispers

  1: slight impairment

26–40 dB

Able to hear and repeat words spoken in normal voice at 1 m

  2: moderate impairment

41–60 dB

Able to hear and repeat words using raised voice at 1 m

  3: severe impairment

61–80 dB

Able to hear some words when shouted into better ear

 4: profound impairment including deafness

81 dB or greater

Unable to hear and understand even a shouted voice

 DURATION OF TRIAL:

The duration of the trial will be 45 days.

 FOLLOW UP:

·      After completion of 45 days of intervention, the patient will be followed for 21 days.

·     Follow-up of the patients will be ensured by telephonic communication or by creating a WhatsApp group. The compliance of the patient will be noted in a separate sheet provided to them.

ASSESSMENT TIME:

Before treatment, the 15th day, the 30th day, and 45th day

Follow-up on the 7th  day and 21st day.

TOTAL DURATION OF TRIAL :

66 days including follow-up.

 INVESTIGATIONS

Following laboratory investigations will be carried out before treatment to rule out any systemic illness,
1. Blood -CBC with ESR
2. Biochemical- RBS

PRIMARY ENDPOINT

 Improvement of air conduction thresholds in patients presenting with hearing loss in the range of 26-60 dB based on pure tone average.

 SECONDARY ENDPOINT

1. Improvement in associated symptoms of Badhirya (SNHL) like Karnanada (Tinnitus)and Bhrama(Giddiness)

2. The study will provide physicochemical and organoleptic properties of Asanabilwadi taila, Ksheerabala taila 101 Avarthi, and Narasimha Choorna.



 
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