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Evaluation of corneal biomechanical alterations and corneal ectasia

Evaluation of corneal biomechanical alterations in keratoconus and pellucid marginal degeneration patients after RGP and ROSE K contact lens wear - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/10/095984
Enrollment
46
Registered
2025-10-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: H186- Keratoconus

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Sankara Eye Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: KCN and PMD patients Eligible for RGP and Rose K CL

Exclusion criteria

Exclusion criteria: C3R surgery Previous RGP and Rose K CL wear Corneal scaring Infectious or inflammatory ocular diseases Corneal graft surgery

Design outcomes

Primary

MeasureTime frame
The corneal stiffness and deformation amplitude changes after 3 months and 6 months of Rose K contact lens wear in keratoconus and pellucid marginal degeneration patients.Timepoint: Baseline 3 months 6 months—

Secondary

MeasureTime frame
The difference in post lens wear changes in the corneal biomechanical properties between RGP and Rose K lenses.Timepoint: Baseline 3 months 6 months—

Countries

India

Contacts

Public ContactVandana Kamath

Sankara Eye Hospital

vandu2388@gmail.com9820541584

Outcome results

None listed

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