QoL Assessment in Traditional Glaucoma Surgery and MIGS.

Quality of Life Assessment in Traditional and Microinvasive Glaucoma Surgery.

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03613233

Enrollment

400

Registered

2018-08-03

Start date

2018-01-01

Completion date

2020-04-01

Last updated

2018-08-03

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

Conditions

Glaucoma

Keywords

MIGS, canaloplasty, glaucoma, glaucoma surgery, glaucoma implant, deep sclerectomy, iridencleisis, QoL, quality of life, NEI VFQ 25

Brief summary

Quality of Life assessment before and after various glaucoma surgery (traditional and microinvasive (MIGS)).

Detailed description

Patients qualified for glaucoma surgical procedure fill in QoL questionnaire (NEI VFQ 25) at baseline (pre-operatively) and 3 months after glaucoma surgery. Additional data will be collected such as demographic data and medical data, visual acuity, intraocular pressure, number of glaucoma medications, stage of glaucoma based on visual field assessment, medical ophthalmic history, intra and postoperative complications, postoperative interventions.

Interventions

PROCEDUREGlaucoma surgery

phacoemulsification

Study design

Allocation

NON_RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

patients qualified for glaucoma surgery in Military Institute of Medicine - based on following Inclusion Criteria: * all glaucoma types with characteristic glaucoma changes (biomicroscopic ,visual field) with documented glaucoma progression * patients not tolerating antiglaucoma medications, * patients with poor compliance * progression in visual field

Exclusion criteria

* active inflammatory disease * pregnancy * mental disease or emotional instability * general steroid therapy * inability to fill in the questionnaire

Design outcomes

Primary

Measure	Time frame	Description
NEI VFQ 25 quality of life score change	baseline (0-30 days; pre-operative) and three months after surgery	NEI VFQ 25 baseline and 3 months after surgery

Countries

Poland

Contacts

Primary ContactAnna Byszewska, MD, PhD

ania.byszewska@gmail.com500285890

Backup ContactMarek Rękas, prof.; MD; PhD

mrekas@wim.mil.pl

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026