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Completed

NCT Number: NCT02114073

Comparison of Effect of Postoperative Cyclosporine A 2% Ophthalmic Emulsion and Betamethasone Eye Drop on Surgical Success of Trabeculectomy Procedure

Glaucoma is one of the leading causes of blindness worldwide and trabeculectomy is the most commonly performed operation to slow-down the disease progression. In this study, we compare the effect of topical cyclosporine A and betamethasone eye drops on the postoperative course and surgical success of trabeculectomy.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Khatam Eye Hospital

Mashhad, Razavi Khorasan Province, 91959-61151, Iran

About this study

Trabeculectomy is still the most popular filtering surgery for glaucomatous patients. In this type of surgery, postoperative care and management is highly important for surgical success. A principle component of postoperative regimen is anti-inflammatory medications. However, corticosteroid eye drops, the most frequently used agents, have some side effects, including raising intraocular pressure.

Cyclosporine A could be an interesting alternative, because not only it has acceptable anti-inflammatory effect and could reduce some ocular surface problems, but also it has minimal direct effect on intraocular pressure. In this study, we will compare the effect of topical cyclosporine A and betamethasone on surgical outcome and postoperative course of trabeculectomy patients.

The study is a prospective study to compare the effect of topical betamethasone and cyclosporine A on postoperative findings of glaucoma patients, undergoing trabeculectomy surgery.

In this study, trabeculectomy patients, who fulfill the study criteria, will be randomized to either study group and follow-up visits will be done in a masked fashion. In each visit, a detailed history taking and eye examination will be done by an examiner unaware of study group. A third party would do data control for patient safety. At the conclusion of the study, the data of the two groups would be compared. All human research ethical codes are strictly respected and the Ethical Committee of the University has an ongoing inspection on all study steps.

We hypothesize that cyclosporine A could provide better inflammation and intraocular pressure control and may enhance surgical success rate. However, our null hypothesis is that the result in study groups will not differ statistically significantly.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • POAG patient with insufficient IOP control on maximal tolerable medical therapy (MTMT), undergoing primary trabeculectomy with MMC augmentation.

Exclusion criteria

  • Age <20 years
  • History of previous ocular surgery in the same eye;
  • Candidate for combined surgery;
  • Pregnancy;
  • Breast feeding;
  • Monocular subject;
  • Allergy to any topical antiglaucoma medication or cyclosporine

Treatment and study plan

cyclosporine

Drug

In study arm, ophthalmic emulsion of cyclosporine A 2% will be prescribed in postoperative phase.

Other names: Cyclosporine A (Sina Darou)

Betamethasone

Drug

In control arm, betamethasone eye drop will be prescribed in postoperative period.

Other names: Betasonate (Sina Darou)

Primary outcomes

  1. Intraocular Pressure (IOP)

    Time frame: Up to 6 months after surgery

    Each month following trabeculectomy, intraocular pressure will be measured using Goldmann Applanation Tonometer.

  2. Bleb morphology

    Time frame: Up to 6 months after surgery

    Bleb morphology according to IBAGS grading system, based on clinical examination and slit-lamp photography.

  3. Subjective dry eye symptoms

    Time frame: Up to 6 months after surgery

    Subjective symptoms of dry eye, reported by patients, and gathered using a standardized questionnaire.

Secondary outcomes

  1. Surgical success rate

    Time frame: 6 month after surgery

    The surgical success rate of trabeculectomy in each study arm.

  2. Complications

    Time frame: Up to 6 months after surgery

    Any complication observed during study period, reported by patient or examiner.

  3. Visual acuity

    Time frame: Up to 6 months after surgery

    LogMAR visual acuity, measured on every postoperative visit.

Sponsors and collaborators

Lead sponsor

Mashhad University of Medical Sciences

Other

Registry information

Official study title

Comparison of Effect of Cyclosporine Ophthalmic Emulsion 2% and Betamethasone Eye Drop on Intraocular Pressure, Conjunctival Hyperemia and Subjective Dry Eye Symptoms Following Trabeculectomy in Open Angle Glaucoma Patients

Acronym: BCATS

Important dates

Study start
2014
Primary completion
2014
Study completion
2015
First posted
Apr 15, 2014
Registry last updated
Apr 21, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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