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Efficacy, safety and patient satisfaction with trans scleral diode laser cyclophotocoagulation (TDLC), for the reduction of intra ocular pressure in glaucoma: A randomised controlled trial.

Efficacy, safety and patient satisfaction with trans scleral diode laser cyclophotocoagulation (TDLC), for the reduction of intra ocular pressure in glaucoma: A randomised controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202406691325176
Enrollment
246
Registered
2024-06-19
Start date
2020-04-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Eye Diseases

Interventions

Medical treatment for advanced glaucoma
Trans scleral diode laser cyclophotocoagulation for advanced glaucoma

Sponsors

Self
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed, advanced POAG patients (vertical cup to disc ratio of 0.9 or more), where the managing consultant recommends either TDLC or medical treatment as primary therapy. 2. All treatment naïve painful blind glaucomatous eyes with elevated IOP where pressure reduction is likely to reduce pain. 3. Adult glaucoma patients aged 18 years and above. 4. Presenting IOP of 28mmHg or more. 5. Known glaucoma patients who have not received any form of glaucoma treatment (medication, laser or trabeculectomy) in the last two months prior to presentation and fulfilling criteria 1-4 above.

Exclusion criteria

Exclusion criteria: 1. Patients with other ocular comorbidities that precludes laser application. 2. Patients who prefer glaucoma medications 3. Patients with uncontrolled systemic diseases like Hypertension, Diabetes mellitus etc. 4. Patients below the age of 18 years

Design outcomes

Primary

MeasureTime frame
Primary outcome was mean intra ocular pressure, IOP, post intervention in both groups as well as percentage reduction in IOP from baseline in the two treatment groups

Secondary

MeasureTime frame
Secondary outcomes for the trial were complication rates, proportion of patients satisfied with treatment as well as proportion of patients loosing two or Snellens lines of presenting visual acuity in the two treatment groups

Countries

Nigeria

Contacts

Public ContactLawan Abdu

Professor Of ophthalmology. MBBS. Msc CEH. MD. FWACS. FMCOphth

lawanabdu25@gmail.com+2348034043804

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026