A clinical trial to study the effect of two formulations Haritkyadi Paryoga and Kampilak Tail Nasya in management of Nasagata Raktapitta w.s.r to Recurrent Epistaxis
Not Applicable
- Conditions
- Health Condition 1: J989- Respiratory disorder, unspecified
- Registration Number
- CTRI/2022/12/048174
- Lead Sponsor
- Principal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients presenting with active epistaxis and/or with history of epistaxis.
Patients having any systemic disease i.e. hypertension, liver disease, kidney disease etc.
Patients who consented to participate.
Exclusion Criteria
Congenital deformity.
Pregnant patients.
Patients not willing to be registered for the trial.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Relief in symptoms in patients of epistaxis.Timepoint: Relief in symptoms in patients of epistaxis.
- Secondary Outcome Measures
Name Time Method To study efficacy of Haritkyadi Prayoga and Kampilak Tail Nasya in improvements in nose bleeding of patients.Timepoint: 2 weeks