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The anticholinergic burden was calculated based on the medications that the patients had used for more than 10 days. Short-term medications used by patients were not evaluated. Among all the medicatio...
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Lead Sponsor
Izmir Ataturk Training and Research Hospital
NCT06812481 · Rheumatoid Arthritis (RA), Anticholinergic Adverse Reaction, and more
NCT07165574 · Frailty in Older Adults, Functional Decline, and more
NCT05538065 · Aging, Benzodiazepine Sedative Adverse Reaction, and more
NCT03698487 · Sedative Adverse Reaction, Anticholinergic Adverse Reaction
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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