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A winter season study in Jaipur on how Haritaki Rasayana supports eye health in older adults.

A Randomized Controlled Trial to Evaluate the Chakshushya Effect of Ritu Haritaki Rasayana in Hemant Ritu in Presbyopic Population of Jaipur. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/103078
Enrollment
74
Registered
2026-02-05
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: H524- Presbyopia

Interventions

None listed

Sponsors

NATIONAL INSTITUTE OF AYURVEDA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: People of Age 35-55 years of either sex or religion Clinical features of presbyopia Difficulty in near vision Asthenopic symptoms Intermittent diplopia for near work

Exclusion criteria

Exclusion criteria: H/O hypersensitivity to the trial drug. Patients having Diabetes and Hypertension. Patients having lenticular or corneal opacity and with any other known ocular pathologies such as optic atrophy, diabetic retinopathy and hypertensive retinopathy. History of recent surgical ocular intervention Contraindication of Haritaki consumption according to Acharya Charaka Ajirni Rukshabhuja Stri madya karshita Ardita Any other condition which the principal investigator thinks may jeopardize the study.

Design outcomes

Primary

MeasureTime frame
Change in Amplitude of Accommodation. Duration of measurement: From baseline and after 8 weeks Method of measurement: Push-up, Push-down and Minus Lens Methods for subjective examination of amplitude of accommodation Timepoint: 8 weeks

Secondary

MeasureTime frame
Gross appearance of eye, Colour vision, Contrast, IOP, Distance visual acuity in presbyopia in presbyopic population. Duration of measurement: From baseline and after every two Suryamana Masa Method of measurement: Visual Acuity test, Slit-lamp examination, Tonometry, Schirmer s Test Timepoint: 8 weeks

Countries

India

Contacts

Public ContactVimleshi Meena

National Institute of Ayurveda

dvd6197@gmail.com7073746600

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026