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Study To Observe The Effect Of Suryabhedana Breathing Exercise In Nasal Blockage

Randomized Controlled Clinical Study To Evaluate The Efficacy Of Suryabhedana Pranayama In The Management Of Nasanaha With Special Reference To Deviated Nasal Septum - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/083512
Enrollment
30
Registered
2025-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: J398- Other specified diseases of upperrespiratory tract

Interventions

None listed

Sponsors

Dr LAKSHMI PRIYA A
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects aged between 21-50 years irrespective of gender, religion, occupation and socioeconomic status will be selected. Subjects presenting with complaints of nasal obstruction, headache, and facial pain. Subjects will be selected based on the Nasal Obstruction and Symptom Evaluation (NOSE) score greater than or equal to 30 (out of a potential score of 100), with 30 defined as a cut off to differentiate subjects with nasal obstruction from those without. Subjects who are fit for doing Suryabhedana Pranayama and Jalaneti. Subjects who are willing to sign the consent form and participate in the study.

Exclusion criteria

Exclusion criteria: Subjects with Nasanaha associated with epistaxis, nasal tumour, septal abscess, sinusitis, nasal polyps and turbinate hypertrophies. Subjects who are contraindicated for Suryabhedana Pranayama and Jalaneti. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Significant improvement in Nasanaha based on changes in SNOT score in comparison to baseline score criteria and also subjective parameters like Obstruction to breathing, headache and facial pain. Timepoint: 1st Assessment 0th day 2nd Assessment 15thday Follow up 30th day

Secondary

MeasureTime frame
Generation of in depth analyzed data on different aspects of disease and its treatment. Improvement in quality of life based on changes in subjective parameter scores. Timepoint: 1st Assessment 0th day 2nd Assessment 15thday Follow up 30th day

Countries

India

Contacts

Public ContactDr LAKSHMI PRIYA A

Sri Sri College of Ayurvedic Science and Research

sajithak96@gmail.com7760987722

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026