An Ayurvedic and Modern Treatment Comparison for Inward Turning of the Eyelid.

A Randomized Controlled Open Clinical Trial Of Agnikarma In Management Of Pakshmakopa With Special Reference To Entropion In Geriatric Group Of 55 to 75 Years. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/102250

Enrollment

Registered

2026-01-28

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Health Condition 1: H020- Entropion and trichiasis of eyelid

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.The patients with symptoms of pakshmakopa 2.Patient of pre-diagnosed and also newly diagnosed pakshmakopa. 3.Patient belonging to any group irrespective of religion, sex, socio-economic class.

Exclusion criteria

Exclusion criteria: 1.Patients having ectropion (outward rolling of eyelids and lashes) 2.Patients with uncontrolled hypertension and diabetes mellitus. 3.Antashonita (Internal bleeding) 4.Anudhrita Shalya (foreign body), Bhiru (coward/sensitive person) 5.Patient not willing to participate in trial. 6.Patients with other diseases such as AIDS, TB, HBsAg that may affect the outcome of result.

Design outcomes

Primary

Measure	Time frame
Following Parameter will be assessed before and after the treatment. 1. Nirvartayanti pakshmani (Misdirected lashes) 2. Foreign body Sensation (Gharshan) 3. Burning Sensation (Daha) 4. Shotha (eye lid swelling) 5. Conjunctival Congestion 6. Corneal Abrasion Timepoint: 3 sittings- 0th, 5th, 10th day. follow up will be taken on 15th and 30th day. 4-5 weeks study.	—

Secondary

Measure	Time frame
1.No improvement - 0 % relief in signs and symptoms. 2.Poor improvement - 0%-25% relief in sign and symptoms. 3.Mild improvement 26% to 50% relief in signs and symptoms. 4.Moderate improvement 51% to 75 % relief in signs and symptoms. 5.Marked improvement 76% to 100% relief in signs and symptoms. Timepoint: 3 sittings- 0th, 5th, 10th day. follow up will be taken on 15th and 30th day. 4-5 weeks study.	—

Measure

Time frame

1.No improvement - 0 % relief in signs and symptoms. 2.Poor improvement - 0%-25% relief in sign and symptoms. 3.Mild improvement 26% to 50% relief in signs and symptoms. 4.Moderate improvement 51% to 75 % relief in signs and symptoms. 5.Marked improvement 76% to 100% relief in signs and symptoms. Timepoint: 3 sittings- 0th, 5th, 10th day. follow up will be taken on 15th and 30th day. 4-5 weeks study.

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Countries

India

Contacts

Public ContactDr Anuja Ashok Ingole

Dayabhai Maoji Majithiya Ayurved Mahavidyalaya and L.K. Ayurved Rugnalaya,Yavatmal.

drharshd@gmail.com9623945054

Outcome results