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NOT YET RECRUITING
NCT06914310
PHASE2/PHASE3

Memantine as an Additive Therapy in Patients With Traumatic Brain Injury

Sponsor: Mansoura University

View on ClinicalTrials.gov

Summary

Memantine has shown promise in mitigating secondary brain injury in previous studies. One study demonstrated that early memantine administration in moderate TBI patients resulted in lower serum neuron-specific enolase levels and improved Glasgow Coma Scale scores. However, other trials investigating memantine's impact on long-term cognitive function in TBI patients have yielded mixed results. There is a need for well-controlled studies to determine the efficacy of memantine in improving neurological and cognitive outcomes in patients with TBI.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2025-03-25

Completion Date

2025-11-30

Last Updated

2025-04-06

Healthy Volunteers

No

Interventions

DRUG

Memantine

Memantine will be given either orally or through a nasogastric tube for 7 days, starting on the first day of admission to the hospital and then continued for 3 weeks. The memantine dose in the first 7 days is 30 mg twice daily, while during the remaining 3 weeks the dose is 10 mg twice daily

DRUG

Mannitol

Mild to moderate TBI patients will receive mannitol in case of brain edema to reduce brain swelling and analgesic for headache such as; acetaminophen.

Locations (1)

Mansoura University

Al Mansurah, Dakahlia Governorate, Egypt