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Clinical trial of Chandanadya varti and Madhukadi lauha churna in presbyopia

CLINICAL EVALUATION OF CHANDANADYA VARTI AND MADHUKADI LAUHA CHURNA IN TIMIRA (AGE RELATED PHYSIOLOGICAL INSUFFICIENCY OF ACCOMMODATION) - Nill

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073764
Enrollment
40
Registered
2024-09-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

None listed

Interventions

None listed

Sponsors

Uttarakhand Ayurved University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient presenting with clinical features of Timira(Age related physiological insufficiency of accommodation) 2.Patient having distant visual acuity 6/6. 3.Patient having near visual acuity ? N6.

Exclusion criteria

Exclusion criteria: 1.Patient having any ocular surface disease (Blepharitis , Dry Eye ,Conjunctivitis , Uveitis , Strabismus , Aphakia , Pseudophakia , Amblyopia ,Corneal infection ,Cataract Glaucoma etc 2.Patient outside the age group 30- 50 years. 3.Patient having other systemic or metabolic disorder.[HTN , DM , THYROID ]

Design outcomes

Primary

MeasureTime frame
Outcome will be measured with the parameters 1.Reduced near vision in dim light 2.Reduced near vision in day light 3.Eye strain 4.HeadacheTimepoint: After trial there will be one follow up after 30 days.—

Secondary

MeasureTime frame
1.Reduced subjective parameters. 2.Reduced objective parameters.Timepoint: After trial there will be one follow up after 30 days.—

Countries

India

Contacts

Public ContactDr Neha Negi

Rishikul Campus, Uttarakhand Ayurved University, Haridwar

gunjan06sharma@gmail.com9258030654

Outcome results

None listed

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