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Study to evaluate outcome of Cataract Surgery with KDB Goniotomy in patients with Glaucoma

Outcome of Phacoemulsification with Kahook Dual Blade Goniotomy in patients with Glaucoma - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/104644
Enrollment
78
Registered
2026-02-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: H409- Unspecified glaucoma

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Nil: Nil Intervention5: Nil: Nil

Sponsors

Rutvi Yogesh Doshi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosed with primary open-angle glaucoma, pseudoexfoliation glaucoma, pigmentary glaucoma, normal tension glaucoma, traumatic glaucoma and combined mechanism glaucoma 2. Underwent Phacoemulsification with intraocular lens implantation with KDB goniotomy from 1st January 2024 in Kasturba Hospital, Manipal by a) Dr. Vijaya Pai H. b) Dr. Neetha K.I.R. 3. Completed 6 months of follow up

Exclusion criteria

Exclusion criteria: 1. Past history of previous glaucoma procedures like trabeculectomy, drainage implant, cyclodestruction procedure or minimally invasive glaucoma surgery in the same eye 2. Neovascular or uveitic glaucoma 3. Incomplete records 4. Intraoperative complications requiring additional glaucoma surgery at the time of surgery 5. Underwent additional glaucoma surgery during the 6 months follow up period

Design outcomes

Primary

MeasureTime frame
1. Changes in Intraocular pressure (IOP) from preoperative baseline. 2. Change in number of antiglaucoma medications.Timepoint: at 1 month and 6 months follow up

Secondary

MeasureTime frame
Success rate of surgery based on IOP control or reduction in the number of anti-glaucoma medications.Timepoint: at 1 month and 6 months follow up;Improvement in BCVA (best corrected visual acuity)Timepoint: at 1 month and 6 months follow up;Incidence of intra-operative and post-operative complications.Timepoint: Intraoperative, at 1 month and 6 months follow up

Countries

India

Contacts

Public ContactRutvi Yogesh Doshi

Kasturba Medical College, Manipal

doshi.kmcmpl2024@learner.manipal.edu918879042911

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026