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A clinical study to see the effect of Ayurvedic formulation in the treatment of black spot in front of eyes.

A randomized clinical trial to evaluate the efficacy of oral administration of Yashtyadi Vati in Dwitiya Patalgata Dosha Dushti with reference to vitreous floaters. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066795
Enrollment
46
Registered
2024-05-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: H433- Other vitreous opacities

Interventions

None listed

Sponsors

Sane Guruji Arogya Kendra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who have signs of Dwitiya Patalgata Dosha Dushti such as black spots, flies, mosquitoes, hairs, squiggly lines or spider webs. 2. Patients between the ages of 19 years to 70 years irrespective of gender, cast and socio-economic condition.[22] 3. Patients who have vitreous floaters on regular basis or suddenly. 4. Patients with both refractive errors – myopic and hypermetropic 5. Asymptomatic patients with high myopia. 6. Patients experiencing eye floaters either before or after any ophthalmic surgery and ophthalmic trauma.

Exclusion criteria

Exclusion criteria: 1. Patients having known case of HIV, Tuberculosis, Rheumatic heart diseases. 2. Patients having known case of Diabetes, Hypertension may interfere with trial group so they are excluded. 3. Patient having history of glaucoma, retinal vein occlusion, macular edema and uveitis. 4. And any condition other than explained in inclusion criteria.

Design outcomes

Primary

MeasureTime frame
To evaluate efficacy of oral administration of Yashtyadi Vati in Dwitiya Patalagat Dosha Dushti w.r.t. Vitreous Floaters assessed on the basis Short Floaters Questioneer.Timepoint: The total duration of trial will be 30 days for each patient with follow up on 0th, 15th and 30 th day. An observational follow up will be done at 45th day. The SFFQ score will be assessed before and after treatment.

Secondary

MeasureTime frame
To compare the efficacy of oral administration of Yashtyadi Vati with Antioxidant tablet in Dwitiya Patalagat Dosha Dushti w.r.t. Vitreous floaters assessed on the basis of Short Floater QuestionnaireTimepoint: Total duration of study is 18 Months

Countries

India

Contacts

Public ContactDr Pravin M Bhat

Sumatibhai Shah Ayurved Mahavidyalaya

vdpravin82@gmail.com09860233173

Outcome results

None listed

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