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Clinical Trials/CTRI/2024/06/068457
CTRI/2024/06/068457Not yet recruitingPhase 2/3

A Comparative Clinical Study on the Efficacy of Karnapoorana and Nasya with Eranda Shigruvadi Tail along with Ghritpana in the Management of Karna Badhirya w.s.r. to Sensorineural hearing loss.

Ayurvedic college Health Department Government of Bihar1 site in 1 country40 target enrollmentStarted: June 18, 2024Last updated:

Trial Snapshot

Phase
Phase 2/3
Status
Not yet recruiting
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
Determination of effect of the intervention

Study Overview

Brief Summary

There are so many drugs against several of health issues are indicated in Ayurveda. One such example is mentioned in Astang Hridyam in their Karna Rogadhikar, where a number of medicines are described among them due to easily formulation and great application of Erand Shigruvadi Taila for Karna Pooran as well as Nasya in our department (dept. of Shalakya Tantra, Govt. Ayurvedic College and Hospital, Patna) have decided that there must be a work has needed on this, so that it can be used as in general practice against the health issues for which it has been indicated in Ayurveda. That is why this work "A Comparative Clinical study on the efficacy of Karna Pooran and Nasya with Erand Shigruvadi Taila along with Ghritpana in the management of Karna Badhirya w.s.r to Sensorineural Hearing Loss (SNHL)" has been proposed.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
None

Eligibility Criteria

Ages
20.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Individual within age group between 20 to 60 years will be included in the study.
  • Patient suffering from sensory neural hearing loss will be selected irrespective of either sex, education, socioeconomic status and religion.

Exclusion Criteria

  • Patients below the age of 20 years and above the age of 60 years.
  • Patient diagnosed with conductive hearing loss.
  • Patient not willing for trial.
  • Pregnant and lactating women.
  • Patients who need surgical and other treatment intervention.
  • Patient suffering from systemic disease.

Outcomes

Primary Outcomes

Determination of effect of the intervention

Time Frame: day7,day14,day21,day28,day35,and day42

Secondary Outcomes

  • Determination of the effect of intervention with respect to other in general(day7,day14,day21,day28,day35 & day42.)

Investigators

Sponsor
Ayurvedic college Health Department Government of Bihar
Sponsor Class
Government medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Shrawan Kumar Gupta

Goverment Ayurvedic college and Hospital Kadamkuan Patna

Study Sites (1)

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