- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT03852810
Satisfaction With XEN Gel Stent Versus Trabeculectomy for the Treatment of Glaucoma (XENPRO)
Patient Reported Outcomes for XEN Gel Stent Versus Trabeculectomy for the Treatment of Glaucoma
Przegląd badań
Status
Warunki
Typ studiów
Zapisy (Rzeczywisty)
Kontakty i lokalizacje
Lokalizacje studiów
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Nova Scotia
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Halifax, Nova Scotia, Kanada, B3H 2Y9
- Dalhousie University
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Ontario
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Kingston, Ontario, Kanada, K7K 6Z6
- Galen Eye Center
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Mississauga, Ontario, Kanada, L5L1W8
- Prism Eye Institute
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Toronto, Ontario, Kanada, M5G 1Z5
- Toronto Ophthalmic Research Innovation Centre, Inc
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Mainz, Niemcy, 55131
- Universitat Augenklinik
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Munich, Niemcy, 80336
- Ludwig-Maximilians-Universität München
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Tübingen, Niemcy
- University of Tubingen
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Cambridge, Zjednoczone Królestwo, CB2 0QQ
- Addenbrooke'S Hospital
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Guildford, Zjednoczone Królestwo
- Royal Surrey County Hospital
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Southend-on-sea, Zjednoczone Królestwo, SS0 0RY
- Southend University Hospital
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Metoda próbkowania
Badana populacja
Opis
Inclusion Criteria:
- Diagnosed with OAG (Open Angle Glaucoma) and using at least 2 topical IOP-lowering medication classes in the study eye
- Scheduled to receive surgical treatment with either XEN (Xen gel stent) or trabeculectomy in the study eye
- Access to an electronic device with internet capabilities and an email address for completion of PROs (Patient Reported Outcomes)
- Be willing and able to complete PROs (Patient Reported Outcomes) at the specified time points
- Able to provide voluntary, informed consent to participate in this study
Exclusion Criteria:
- Diagnosed with angle closure glaucoma in the study eye
- Presence of a secondary glaucoma, pseudoexfoliation glaucoma, or pigmentary glaucoma
- Presence of neovascular, uveitic, or angle recession glaucoma or any glaucoma associate with vascular disorders
- Prior incisional glaucoma surgery, canal-based surgery, suprachoroidal space-based surgery (trabeculectomy, viscocanalostomy, canaloplasty, shunts of any type, collagen implants, etc.) or a cilio-ablative procedure
- Clinically significant inflammation or infection in the study eye within 30 days prior to the baseline visit (e.g. blepharitis, conjunctivitis, keratitis, uveitis, herpes simplex infection)
- History of corneal surgery, corneal opacities, or corneal disease
- Prior intraocular surgery in either eye ≤ 3 months prior to study enrollment with the exception of uncomplicated cataract surgery in either eye ≥ 1 month prior to study enrollment
- Anticipated ocular surgery in either eye within 6 months of baseline
- Concomitant cataract surgery scheduled at the time of glaucoma procedure
The study eye is defined as the eye receiving surgical intervention with either XEN or trabeculectomy.
Patients who have received prior laser trabeculoplasty will be permitted to participate if all other inclusion/exclusion criteria are met.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
Kohorty i interwencje
Grupa / Kohorta |
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Receiving surgical intervention via XEN Gel Stent (XEN)
Patient Reported Outcomes (PRO) will be collected before and after this particular procedure
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Receiving surgical intervention via trabeculectomy
Patient Reported Outcomes (PRO) will be collected before and after this particular procedure
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
---|---|---|
To evaluate and compare the visual function and local eye symptoms in patients receiving surgical intervention via XEN (Xen gel stent) or trabeculectomy.
Ramy czasowe: 3 Months
|
Visual function and local eye symptoms using the Glaucoma Symptom and Health Problem Chart (SHPC-18) SHPC-18 is an eighteen question survey to assess local eye and visual function symptoms caused by glaucoma or its treatments. The tool is comprised of 7 questions related to local eye symptoms, and 11 related to visual function problems. The 2-domain tool is a psychometrically validated measure of patient-reported, glaucoma-related symptoms that is responsive to treatment and discriminates the severity of glaucoma to better understand the influence of glaucoma symptoms on patients' daily life. |
3 Months
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
---|---|---|
To evaluate and compare the treatment satisfaction and expectations in patients receiving surgical intervention via XEN and trabeculectomy.
Ramy czasowe: 3 Months
|
Patients treatment satisfaction and expectations will be measured using a study specific Glaucoma Surgery Satisfaction Survey.
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3 Months
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To evaluate and compare work productivity in patients receiving surgical intervention via XEN and trabeculectomy.
Ramy czasowe: 3 Months
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Work productivity using the Work Productivity and Activity Impairment Questionnaire: Specific Health Problem v2.0 (WPAI:SHP) The WPAI is a six question survey to quantitatively assess the amount of absenteeism, presenteeism, and daily activity impairment attributable to specific health problems. Participants will be asked about their employment status, the amount of hours they have missed due to their health problems, the amount of hours they have missed due to non-health problems, how many hours they worked, how much their health problems affected work productivity, and how much their health problems affected their regular daily activities for the recall period of one week |
3 Months
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To evaluate and compare the visual acuity recovery time in patients receiving surgical intervention via XEN and trabeculectomy.
Ramy czasowe: 3 Months
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Visual acuity will be recorded from the patient chart and converted from the site-specific metric to EDTRS letter equivalents
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3 Months
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To evaluate and compare the refractive change from baseline in patients receiving surgical intervention via XEN and trabeculectomy.
Ramy czasowe: 3 Months
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3 Months
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To evaluate and compare the IOP (Intraocular Pressure) change from baseline in patients receiving surgical intervention via XEN and trabeculectomy.
Ramy czasowe: 3 Months
|
3 Months
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To evaluate and compare new onset ocular hypotensive medication use in patients receiving surgical intervention via XEN and trabeculectomy.
Ramy czasowe: 3 Months
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3 Months
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To present glaucoma procedure-related adverse events in patients receiving surgical intervention via XEN and trabeculectomy.
Ramy czasowe: 3 Months
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3 Months
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To evaluate glaucoma related healthcare resource utilization (HRU) by the mean number of physician office visits
Ramy czasowe: 3 Months
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3 Months
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To present post-operative medical management in patients receiving surgical intervention via XEN and trabeculectomy.
Ramy czasowe: 3 Months
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3 Months
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To evaluate glaucoma related healthcare resource utilization (HRU) by medication use
Ramy czasowe: 3 Months
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3 Months
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To present post-operative surgical management in patients receiving surgical intervention via XEN and trabeculectomy
Ramy czasowe: 3 Months
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3 Months
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Współpracownicy i badacze
Sponsor
Śledczy
- Dyrektor Studium: Joanna Campbell, Ph.D, Allergan
Publikacje i pomocne linki
Przydatne linki
- To be considered as a site for current and future Allergan Clinical Trials, please register using the Investigator Databank link.
- Additional information on study locations near you may be found at AllerganClinicalTrials.com. For any study not on AllerganClinicalTrials.com, please contact IR-CTRegistration@Allergan.com for assistance
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- P-2016-6380
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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