A study to compare effect of vacha pippali nasya and yashtimadhu madhu nasya in suryavarta( frontal sinusitis)

A comparative clinical study to evaluate the efficacy of yashtimadhu madhu avapeeda nasya with vacha pippali avapeeda nasya in suryavarta( frontal sinusitis)

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/06/043219

Enrollment

Registered

2022-06-13

Start date

Unknown

Completion date

Unknown

Last updated

2022-10-17

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

Conditions

Health Condition 1: J011- Acute frontal sinusitis Health Condition 2: J321- Chronic frontal sinusitis

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient within the age group of 16 to 60 years who will give their written consent 2. pt who will agree to follow protocol of study 3.subjects with symptoms of: a)shirashoola dinavruddha b) lalataruk c)akshiruk d)shankaruk e)spandanavat vedana f)tenderness over sinus area

Exclusion criteria

Exclusion criteria: 1)Subjects with complications of sinusitis. 2)Pregnant and lactating women. 3)Headaches with involvement of other intracranial pathology. 4)Subjects contraindicated for nasya. 5)Patients with other systemic illness.

Design outcomes

Primary

Measure	Time frame
The effect of treatment will be assessed based on detailed case proforma adopting methods of subjective parameters such as site, intensity and nature of pain. And also according to objective criteria like tenderness over sinus area and ESR. Pre and post interventional assessment will be doneTimepoint: The effect of treatment will be assessed before treatment( day 0), after treatment( day 7) and on day 14, 21 and 52	—

Measure

Time frame

The effect of treatment will be assessed based on detailed case proforma adopting methods of subjective parameters such as site, intensity and nature of pain. And also according to objective criteria like tenderness over sinus area and ESR. Pre and post interventional assessment will be doneTimepoint: The effect of treatment will be assessed before treatment( day 0), after treatment( day 7) and on day 14, 21 and 52

—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDr Apeksha D Rao

Alvas ayurveda medical college, affiliated with RGUHS

drapekshadrao@gmail.com7411360991

Outcome results