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A clinical study to evaluate the efficacy of shodhana navana nasya and avapeedana nasya in manyastambha

Phase 3
Conditions
Health Condition 1: M488- Other specified spondylopathies
Registration Number
CTRI/2020/04/024794
Lead Sponsor
Dr Haripriya Vasudev
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1 Subjects with clinical signs and symptoms of manyastambha.

2 Age between 21-50 years old.

3 Subjects of either gender irrespective of religion and socio economic status.

4 Subjects fit for nasya

Exclusion Criteria

1 Pregnant and lactating women.

2 Subjects with congenital deformity, traumatic injury, cervical stenosis and myelopathy, infections of bone and gross bony deformity and epistaxis.

3 Other systemic disorders which interfere in the line of treatment like uncontrolled diabetes, uncontrolled hypertension and cardio vascular disease.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
There is no significant difference in the outcome of both shodhana navana nasya and avapeedana nasya.Timepoint: 7th day <br/ ><br>14th day
Secondary Outcome Measures
NameTimeMethod
Shodhana navana nasya is better than avapeedana nasyaTimepoint: 7th day <br/ ><br>14th day
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