Skip to content

Role of Saindhavadya Anjana and Carboxy Methyl Cellulose eye drop with Jeevaniya Taila Nasya for treating Shushkakshipaka with special reference to Computer Vision Syndrome

A randomized comparative clinical trial on the efficacy of Saindhavadya Anjana and Carboxy Methyl Cellulose eye drop each combined with Jeevaniya Taila Nasya in the management of Shushkakshipaka with special reference to Computer Vision Syndrome

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093845
Enrollment
100
Registered
2025-08-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: H539- Unspecified visual disturbance

Interventions

None listed

Sponsors

National Institute of Ayurveda Deemed to be University (De-novo) Jaipur (Raj.)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients between 18 to 55 years of age and willing to participate in this study through written consent are recruited. 2.Patients utilizing a Computer or Video Display Terminals VDTs for a minimum of two hours each day and presenting with minimum three of clinical features of Shushkakshipaka Computer Vision Syndrome such as Kunita Vartma Photophobia, Avila Darsana Blurring of vision, Gharsa Foreign body sensation, Toda Asthenopia, Ushnadaha Burning sensation, Vishushkatva Dryness of eyes, Raga Conjunctival congestion. 3.Patients with OSDI score from Mild 13 to 22 to Moderate 23 to 32 will be included in the study.

Exclusion criteria

Exclusion criteria: 1.Individuals under the age of 18 and those over the age of 55 are not included in the study. 2.Cases that are complicated by Acute or Chronic infection of Conjunctiva, Eyelid, Cornea, Dacryocystitis, Lagophthalmos, Sjogrens Syndrome. 3.Pregnant and lactating women are excluded in the study. 4.Patients with severe systemic illnesses that could hamper the trial in between are excluded. 5.Severe patients of Computer Vision Syndrome with complications like Corneal Ulcer.

Design outcomes

Primary

MeasureTime frame
Changes in Ocular Surface Disease Index (OSDI) score in Shushkakshipaka (Computer Vision Syndrome).Timepoint: Improvement in OSDI score from baseline to the end of 33 days treatment period, indicating relief in Shushkakshipaka (Computer Vision Syndrome).

Secondary

MeasureTime frame
Changes in Schirmer-1 reading, Tear Film Break-Up Time, Ocular Surface Staining grading and subjective Ocular symptoms grading in Shushkakshipaka (Computer Vision Syndrome).Timepoint: Improvement in Schirmer-1 reading, Tear Film Break-Up Time, Ocular Surface Staining grading and subjective Ocular symptoms grading from baseline to the end of 33 days treatment period, indicating relief in Shushkakshipaka (Computer Vision Syndrome).

Countries

India

Contacts

Public ContactDr Mahima Choudhary

National Institute of Ayurveda Deemed to be University (De-novo) Jaipur

pamnani.gulab@gmail.com9461154942

Outcome results

None listed

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