Cognitive and Behavioral Impairment

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Review clinical trials related to Cognitive and Behavioral Impairment. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Evaluation of the Effect of L-Arginine on the Cognitive Function in Geriatric Patients

This study aims to evaluate the effect of L-arginine supplementation on cognitive function in geriatric patients. Eligible participants will receive either L-arginine (6 grams once daily) or placebo, and their cognitive performance will be assessed using validated cognitive assessment tools over the study period. The participants will receive the intervention for 4 weeks and followed up every 2 weeks. The primary outcome is improvement in cognitive function, while secondary outcomes include safety, tolerability, and quality of life measures. The findings may provide evidence for the potential role of L-arginine in supporting cognitive health in elderly populations.

Participants needed: 60
Trial details
Phase: Phase 2Age: 60+Biological sex: AllType: InterventionalSponsor: German University in CairoUpdated: Jan 21, 2026Locations: 1
Eligibility criteria

Age >60 years [+1]

Presence of neurodegenerative diseases (e.g.: Alzheimer's disease, Parkinson's d... [+11]

Status: Recruiting

Incidence of Postoperative Cognitive Decline in Patients With Preexisting Cognitive Impairment

This study aims to find out how often memory and thinking problems happen after surgery in people who already have memory issues before their operation. These memory problems are called postoperative cognitive decline (POCD). Older adults with memory problems before surgery may be more likely to have trouble with thinking, memory, and daily activities after their operation. This study will follow patients who already have memory problems before surgery and see how their thinking and memory change after surgery. The results will help doctors better understand how to care for these patients before, during, and after surgery.

Participants needed: 340
Trial details
Age: 60+Biological sex: AllType: ObservationalSponsor: Peking University Shenzhen HospitalUpdated: Aug 22, 2025Locations: 1Duration: 1 Year
Eligibility criteria

Preexisting Cognitive Impairment (PreCI) Surgical Group [+3]

Expected difficulty in completing neuropsychological assessments (e.g., inabilit... [+9]