Swedish Microinvasive Glaucoma Surgery Study (SMIGS)
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- STATUS
- Recruiting
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- End date
- Sep 5, 2027
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- participants needed
- 120
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- sponsor
- Umeå University
Summary
The purpose of the study is to investigate the efficacy of Cataract Surgery as stand-alone compared to Cataract Surgery in combination with Kahook Dual Blade Glide goniotomy (KDB) or iStent Inject W Trabecular Microbypass Stent (Istent) in eyes with Open-angle glaucoma.
Description
Glaucoma patients with significant cataract are being informed about the study and potential risks, all participants giving written informed consent and meeting the criteria will become eligibility for study entry. Participants meeting the eligible requirements will be randomized to Cataract Surgery as stand-alone (40 patients) or Cataract Surgery combined with Kahook Dual Blade Glide (40 patients) or iStent Inject W (40 patients).
Details
| Condition | Open Angle Glaucoma, MIGS, Goniotomy, Istent Inject W, Cataracts, Kahook Dual Blade Glide, Glaucoma, Cataract, Pigmentary glaucoma |
|---|---|
| Treatment | cataract surgery, iStent, KDB |
| Clinical Study Identifier | NCT05035394 |
| Sponsor | Umeå University |
| Last Modified on | 5 October 2021 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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