To study the effect of kantakari avaleha in kasa with investigation of total leukocyte count

Single arm clinical study to assess the effect of Kantakari Avaleha in Kasa with special reference to Total Leukocyte Count - Nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/08/072072

Enrollment

Registered

2024-08-07

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: R05- Cough

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients with acute onset of Kasa of less than two Weeks duration was included. Patients have fulfilling criteria for diagnosis of Cough, Shirshool, Parshvashol , Uroshool, Daha, Kantha Kandu , Peenasa

Exclusion criteria

Exclusion criteria: Patient of Kshataj and Kshayaj Kasa. Pregnant and lactating women Known case of Chronic obstructive Pulmonary disease, pneumonia, Bronchiectasis, lung abscess, pulmonary edema, HIV, HBsAg

Design outcomes

Primary

Measure	Time frame
To decrease the signs and symptoms of Kasa Timepoint: 21 days study with follow up on 7th, 14th,and 21st day	—

Secondary

Measure	Time frame
To study the adverse effect of Ayurvedic formulation, if any.Timepoint: 21 days study with follow up on 7th,14th & 21st day	—

Countries

India

Contacts

Public ContactDr Gauri Atmaram Mulik

LRP Ayurvedic Medical College and Hospital

gaurimohite492@gmail.com8806073556

Outcome results