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This study aims to characterize patients with diabetic macular edema (DME), their progression, the treatment received and associate the functional and physiological outcomes related to the treatment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with diabetic macula edema (DME) | Patients diagnosed with diabetic macula edema (DME) in at least one eye, at least 18 years old, with information on laterality and registered in the Vestrum health database between January 2015 and May 2023. |
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| Measure | Description | Time Frame |
|---|---|---|
| Change in visual acuity | From January 2015 to April 2023 | |
| Progression to DME in the fellow eye | From January 2015 to April 2023 | |
| Initial treatment of DME | From January 2015 to April 2023 | |
| Central retinal thickness (CRT) | From January 2015 to April 2023 |
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Inclusion Criteria:
All patients ≥18 years, with a DME diagnosis in at least one eye, included in the Vestrum database identified during the study period (January 2015 to April 2023)
Exclusion Criteria:
Patients without the information of laterality will be excluded.
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The study population is based on the patients attending a retinal specialist, included in the Vestrum Retinal specialist database. The study population will include adult patients with a DME diagnosis in at least one eye.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CorEvitas HQ | Waltham | Massachusetts | 02451 | United States |
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| Label | URL |
|---|---|
| Related Info | View source |
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Clinical studies sponsored by Boehringer Ingelheim, phases I to IV, interventional and non-interventional, are in scope for sharing of the raw clinical study data and clinical study documents. Exceptions might apply, e.g. studies in products where Boehringer Ingelheim is not the license holder; studies regarding pharmaceutical formulations and associated analytical methods, and studies pertinent to pharmacokinetics using human biomaterials; studies conducted in a single center or targeting rare diseases (in case of low number of patients and therefore limitations with anonymization).
For more details refer to:
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