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Indications and clinical outcomes of Pinhole Pupilloplasty (PPP)

A Prospective Analysis of Surgical Indications and Clinical Outcomes of Pinhole Pupilloplasty (PPP) Technique - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097729
Enrollment
25
Registered
2025-11-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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 Health Condition 2: H178- Other corneal scars and opacities Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: Pinhole Pupilloplasty (PPP): Pinhole Pupilloplasty (PPP) will be performed under peribulbar anaesthesia using the Single-Pass Four Throw (SFT) Technique by a single surgeon. Participant

Sponsors

Mehul Ahlawat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 18 to 80 years, willing to consent, with visually significant symptoms like glare, photophobia, monocular diplopia attributable to irregular corneal topography, irregular pupils, Urretes Zavalia Syndrome, and prescence of adequate iris tissue for suturing.

Exclusion criteria

Exclusion criteria: Age less than 18 yrs, central corneal scar or opacity, active ocular infection, pre existing glaucoma, posterior segment pathology limiting visual potential, iris atrophy, one eyes patient, unable to give consent and comply with follow up schedule.

Design outcomes

Primary

MeasureTime frame
Primary clinical indications for performing pinhole pupilloplasty. To document preoperative clinical parameters and compare postoperative outcomes in terms of a.Uncorrected and Best-corrected visual acuity b.Contrast sensitivity c.Strehl Ratio d.RMS values Total, Astigmatism, Spherical, Coma and Trefoil aberrations. e. Subjective symptom relief using Iris Glare, Appearance and Photophobia Questionnaire. f. Pupil centration and size. To document intraoperative and postoperative complications.Timepoint: Baseline, Post Operative Day (POD) 1, 1 week, 1 month, 3 months.

Secondary

MeasureTime frame
NILTimepoint:

Countries

India

Contacts

Public ContactTushya Om Parkash

Dr. Om Parkash Eye Institute

tushya@aol.in9980813156

Outcome results

None listed

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