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Comparing single versus combined procedure in pseudoexfoliation glaucoma

PSEUDOEXFOLIATIVE GLAUCOMA-Comparing efficacy of PHACOEMULSIFICATION VERSUS PHACOTRABECULECTOMY - None

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021543
Enrollment
50
Registered
2019-10-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: H408- Other glaucoma

Interventions

Intervention1: Phaco or Phacotrab: Include pts who already have undergone cataract or combined phaco+trabeculectomy surgery Control Intervention1: None-Not applicable: Phaco versus phacotrab

Sponsors

LV Prasad Eye Institute MTC campus
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Medically controlled cases of XFG with visually significant cataract Age > 40years With or without raised IOP Underwent either phaco/phacotrabeculectomy Pseudoexfoliation syndrome would include adults >40 years with visually significant cataract, with evident classical dandruff or flaky exfoliation deposits on the pupil, lens or other ocular structures, radial pigment over the lens surface with or without raised intraocular pressure. Ocular hypertension are those with raised IOP with normal optic nerve and visual field while glaucoma would be defined as those with glaucomatous optic neuropathy evidenced by cupping, rim thinning, notch or retinal nerve fibre layer defects with or without corresponding visual field defects

Exclusion criteria

Exclusion criteria: 1.Ocular history of any prior incisional procedure( apart from phaco/phacotrab) 2. Medically uncontrolled IOP 3. Retinal or neurologic disease 4.H/O of any trauma to the eyes 5.Secondary glaucoma

Design outcomes

Primary

MeasureTime frame
IOP reduction from 0 and every 3-4 months till 2 years after surgery VF status at final follow up comparison to baseline and immediately before surgery Timepoint: 0, 3months, 6months, 1 year, 1.5 years and 2 years at final follow up

Secondary

MeasureTime frame
Intra and postoperative complications Postoperative interventions IOP spikes and postoperative hypotony-complication Timepoint: every 3months after surgery-3,6,9,12,15,18,24 months until completion

Countries

India

Contacts

Public ContactRakhi D cruz

LV Prasad Eye Institute, MTC campus

vinodini10375@yahoo.com07894393705

Outcome results

None listed

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