A clinical study to see the effect of Ayurvedic formulation in the treatment of childrens farsightedness(Paediatric Myopia)

A randomized controlled trial to evaluate efficacy of oral administration of Shadang Kwath Vati with spectacles in Pratham Dwitiya Patalagata Timir with reference to Paediatric Myopia - Nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/086656

Enrollment

Registered

2025-05-09

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Conditions

Health Condition 1: H521- Myopia

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patient Enrolled with symptoms of Prathama-Dwitiya Patalagata Timira i.e. Avyaktam- ekshateroopam (visual hallucination), Vyaktamapyanimitta (transient nature of blurriness), Dooram-n-ekshate (difficulty of distant vision) in Shalakya OPD. 2)Age- 08 to 16 years.

Exclusion criteria

Exclusion criteria: 1)Patient who have symptoms of Tritiya and Chaturtha Patalagata Timira will be excluded 2)Congenital type of myopia, pathological type of myopia, acquired or secondary type of myopia that occurs due to some factors or diseases i.e. post traumatic, drug induced, post keratitis. etc. will be excluded 3)Myopia associated with other ocular diseases like cataract, glaucoma,etc 4)Patient who have myopia associated with other refractive errors such as astigmatism 5)Patient who have known case of hypertension, diabetes mellitus, Rheumatic arthritis or any other arthritic conditions, rheumatic heart disease, thyroid disorder, asthma, Koch s, HIV will be excluded 6)Patient who have active infectious diseases i.e. viral, fungal, bacterial conjunctivitis, trachoma, blepharitis

Design outcomes

Primary

Measure	Time frame
To study the efficacy of oral administration of Shadang Kwath Vati in the management of Pratham Dwitiya Patalagata Timir with reference to Paediatric Myopia which will be assesed on the basis of visual acuity with uncorrected and best corrected visual acuity. Timepoint: The total duration of treatment for each patient will be 30 days with follow up on 0th, 15th and 30th day with an observational follow up on 45 th day. The effect will be assessed before and after treatment on the basis of uncorrected and best corrected visual acuity.	—

Measure

Time frame

To study the efficacy of oral administration of Shadang Kwath Vati in the management of Pratham Dwitiya Patalagata Timir with reference to Paediatric Myopia which will be assesed on the basis of visual acuity with uncorrected and best corrected visual acuity. Timepoint: The total duration of treatment for each patient will be 30 days with follow up on 0th, 15th and 30th day with an observational follow up on 45 th day. The effect will be assessed before and after treatment on the basis of uncorrected and best corrected visual acuity.

—

Secondary

Measure	Time frame
To compare the efficacy of oral administration of Shadang Kwath Vati with a spectacles in Pratham Dwitiya Patalgata Timira w.r.t. Paediatric Myopia which will be assessed on the basis of Visual Acuity under uncorrected & best corrected visual acuity.Timepoint: Total duration of study is 18 Month	—

Countries

India

Contacts

Public ContactDr Sumedha Y Kotangale

Sumatibhai shah Ayurvedic Medical College Malwadi Hadapsar Pune 411028

sumedhayk@yahoo.com8275298480

Outcome results