Clinical efficacy of Hopea parviflora Bedd. in Alasa( Tinea pedis)

Pharmacognostical,Phytochemical study of Hopea parviflora Bedd. and its clinical efficacy in Alasa (Tinea pedis) - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/065641

Enrollment

Registered

2024-04-15

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

Health Condition 1: L088- Other specified local infections of the skin and subcutaneous tissue

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex, between the age group of 16-60 years who will fulfill the diagnostic criteria will be taken up for the study

Exclusion criteria

Exclusion criteria: Patients suffering from systemic diseases, Patients taking immuno-suppresive medications, lesions with secondary infections

Design outcomes

Primary

Measure	Time frame
patient will be assessed on the improvement in clinical features. pateints will be assessed as per the subjective parameters- kandu(pruritis), Daha( burning sensation), Ruja( pain) and objective parameters- maceration and fissuring.Timepoint: patients will be assessed once in 7 days i.e. on 7th, 14th, 21st, 28th day.	—

Secondary

Measure	Time frame
Patient will be assessed on the improvement in clinical features.Timepoint: patient will be assessed once in 14days during the follow up period	—

Countries

India

Contacts

Public ContactDrKshama Jain

Alvas Ayurveda medical College and Hospital,Moodabidri, DK district

drsp28@gmail.com9448327156

Outcome results