A Comparative Clinical Study To Evaluate The Efficacy Madhu Shigrupallava Swarasa Aschyotana( Honey drumstickleaves freshjuice eyedrops) And Madhu Shigrupallava Arka Aschyotana(Honey drumstickleaves distillate eyedrops) In The Management Of Vataja Abhishyanda W S R To Allergic Conjunctivitis

A Comparative Clinical Study To Evaluate The Efficacy Of Madhu Shigrupallava Swarasa Aschyotana And Madhu Shigrupallava Arka Aschyotana In The Management Of Vataja Abhishyanda W S R To Allergic Conjunctivitis

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/01/016961

Enrollment

Registered

2019-01-08

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: H108- Other conjunctivitis

Interventions

Intervention1: MADHU SHIGRUPALLAVA SWARASA ASCHYOTANA: MADHU SHIGRUPALLAVA SWARASA ASCHYOTANA 10 DROPS FOR EACH EYE FOR 14DAYS Control Intervention1: MADHU SHIGRUPALLAVA ARKA ASCHYOTANA: MADHU

Eligibility

Inclusion criteria

Inclusion criteria: PATIENTS OF EITHER SEX AGED BETWEEN 17 TO 55 YEARS PATIENTS PRESENTING WITH LAKSHANAS OF VATAJA ABHISHYANDA PATIENTS PRESENTING WITH SIGNS AND SYMPTOMS OF ALLERGIC CONJUNCTIVITIS

Exclusion criteria

Exclusion criteria: PATIENTS WITH COMPLICATIONS LIKE MARGINAL CORNEAL ULCER TRACHOMA DACRYOCYSTITIS KERATOCONJUNCTIVITIS AND OTHER OCULAR INFECTIONS PATIENTS SUFFERING FROM OTHER SYSTEMIC DISEASES WHICH INTERFERE WITH THE COURSE OF TREATMENT

Design outcomes

Primary

Measure	Time frame
EFFICACY OF INTERVENTION OVER SUBJECTIVE AND OBJECTIVE CRETIRIA OF VATAJA ABHISHYANDA WSR TO ALLERGIC CONJUNCTIVITISTimepoint: ONE YEAR	—

Secondary

Measure	Time frame
NILTimepoint: NA	—

Countries

India

Contacts

Public ContactDR SUJATHAMMA K

SRI KALABYRAVESHWARA SWAMY AYURVEDIC MEDICAL COLLEGE HOSPITAL AND RESEARCH CENTRE

drsujathammaskamc@gmail.com9448848786

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026