A study to evaluate the effect of Nasya and gandusha in snoring.

A CLINICAL STUDY OF NASYA WITH ANU TAILA AND GANDUSHA WITH DARUHARIDRA KWATH IN MANAGEMENT OF SHALUKA (SNORING) - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/08/056350

Enrollment

Registered

2023-08-09

Start date

Unknown

Completion date

Unknown

Last updated

2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J399- Disease of upper respiratory tract, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patient suffering from classical sign and symptoms of shaluka (Snoring) 2)Patient between 20 year to 55 year of age. 3)Patient willing and able to participate in the study for 21 days and follow up.

Exclusion criteria

Exclusion criteria: 1)Pregnant and lactating woman. 2)Subjects contra-indicated for Nasya and GANDUSHA. 3)Patient suffering from severe systemaic disorders like HTN ,D.M. 4)Patients suffering with other systemic chronic disorders like Malignancy, Cardiac and Renal disease. 5)Patient suffering from gross deviation of nasal septum and associated with other nasal pathology like nasal polyps etc. 6)Patient suffering from other infectious diseases. 7)Patient suffering from obstructive sleep apnea.

Design outcomes

Primary

Measure	Time frame
Change in subjective parameter according to THORNTON SNORING SCALE.Timepoint: 51 Days	—

Secondary

Measure	Time frame
To improve the quality of life .Timepoint: 51 Days	—

Countries

India

Contacts

Public ContactDr Gyan Prakash Sharma

Post Graduate Institute of Ayurveda, DSRRAU, JODHPUR

atreyagyan@gmail.com9829798701

Outcome results