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Status unknownNCT05437614Updated Jun 29, 2022

Comparison of Outcome and Effectiveness Between Micropulse Diode Laser Cyclophotocoagulation and Cyclocryoablation in Treatment of Refractory Glaucoma

An interventional study of Micropulse diode laser cyclophotocoagulation in treatment of refractory Glaucoma and Cyclocryoablation in treatment of refractory Glaucoma in Treatment of Refractory Glaucoma, sponsored by University of Health Sciences Lahore. Status unknown at 1 site in Pakistan. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-06-29.

Sponsored by University of Health Sciences Lahore · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jun 2022), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Mar 2022, registered Jun 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
47
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

laucoma having bad prognosis after maximally tolerated medication,glaucoma that fails after filtering operations, neovascular glaucoma, glaucoma following vitrectomy and glaucoma secondary to uveitis etc. is collectively termed as refractory glaucoma. For such glaucoma patients, cyclodestructive procedures are often used to reduce IOP, as well as to relieve ocular and periocular pain. Recently,diode laser transscleral cyclophotocoagulation has proved to be an effective method for the treatment of refractory glaucoma and it has become a standard treatment for refractory glaucoma.(Yu, Q., Liang, Y., Ji, F. and Yuan, Z.,et al 2020. ) In previous articles, little is known about the long-term outcomes of micropulse diode laser cyclophotocoagulation and cyclocryotherapy. Discrepancies in the results of several large observational analyses have introduced further ambiguity on the role of micropulse diode laser cyclophotocoagulation and cyclocryotherapy.The mechanism of transcleral cyclophotocoagulation IOP lowering in refractory glaucoma is not well understood. In this study, we perform cyclocryoablation and micropulse diode laser cyclophotocoagulation in patients with refractory glaucoma and report the outcomes / mechanism of IOP control using this new surgical paradigm. The objective of our project is to assess the end result and outcome of the role of micropulse diode laser cyclophotocoagulation and cyclocryotherapy.We aim to evaluate the comparison between micropulse diode laser cyclophotocoagulation and cyclocryotherapy.

Only those subjects will be recruited who provide written informed consent. Patients are diagnosed on bases of tonometry, gonioscopy, ophthalmoscopy, perimetry. Patients' age, gender, type of glaucoma, number of diode laser treatment sessions, postoperative complications, number of hypotensive medications required to control IOP, and best corrected visual acuity (BCVA) will be evaluated. The criteria for success will be defined as postoperative IOP \<21 mmHg or >20% decrease in IOP with or without additional medical treatment.

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Conditions studied

  • Treatment of Refractory Glaucoma

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03

In context

Glaucoma

1,818 studies on the registry are indexed under Glaucoma; 231 are open to participants now.

This study's planned enrollment of 47 is below the median of 65 across 1,272 interventional studies indexed under Glaucoma.

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Lead sponsor

University of Health Sciences Lahore is the lead sponsor of 77 studies on the registry; 49 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Positive diagnosis of refractory glaucoma

  • Poor visual acuity: Hand movements or less
  • Age ≥ 18 years
  • Intraocular pressure ≥ 21 mmHg
  • Signed informed consent

Exclusion criteria

Exclusion Criteria:

  • Eye surgery performed over the last 3 months
  • Eye inflammation
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
47 participants (estimated)

Study arms

  • Active comparator
    Treatment of refractory glaucoma using Micropulse diode laser cyclophotocoagulation

    Procedure: Micropulse diode laser cyclophotocoagulation in treatment of refractory Glaucoma

  • Active comparator
    Treatment of refractory glaucoma using cyclocryoablation

    Procedure: Cyclocryoablation in treatment of refractory Glaucoma

Interventions

  • ProcedureMicropulse diode laser cyclophotocoagulation in treatment of refractory Glaucoma

    Treatment of refractory Glaucoma by Micropulse diode laser cyclophotocoagulation

  • ProcedureCyclocryoablation in treatment of refractory Glaucoma

    Treatment of refractory Glaucoma by cyclocryoablation

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What researchers measure

Primary outcomes

  1. postoperative complications

    Hypotony, Fibrinous uveitis, Cystoid macular edema

    Time frame: 1 year

  2. Reduced IOP

    Reduction in IOP to less than 21 mmHg medications required to control IOP

    Time frame: 1 year

  3. Decrease in number of hypotensive drugs

    Time frame: 1 year

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Study locations

1 of 1 sites recruiting
  • Holy Family Hospital
    Rawalpindi, Punjab 46000, Pakistan
    Recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 29, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05437614
Lead sponsor
University of Health Sciences Lahore
Responsible party
Mariam Noor (Post Graduate Trainee, University of Health Sciences Lahore) — Principal investigator
First posted
Jun 29, 2022
Start date
Mar 1, 2022
Primary completion
Sep 1, 2022 (estimated)
Completion
Mar 1, 2023 (estimated)
Last update
Jun 29, 2022

Study contacts

Mariam Noor, MBBS
Contact
drmariam133@gmail.com
923314512003

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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