CompletedPhase 3

The Effect of Mannitol Volume with Changes in Osmolarity in Traumatic Brain Injury

Indonesia32 participantsStarted 2023-11-01

Plain-language summary

This observational study is designed to research the effect of mannitol volume administration with changes in osmolarity in patients with traumatic brain injury to guide the safe use of mannitol in these patients.

Who can participate

Age range18 Years – 40 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients aged 18-40 years * Glasgow Coma Scale (GCS) score indicating mild (14-13) or moderate (12-10) Exclusion Criteria: * Renal impairment * Multiple trauma with bleeding shock * Diabetes mellitus

What they're measuring

Osmolarity

Timeframe: At baseline (before administration) and subsequently at 6 hours and 24 hours post-administration

Trial details

NCT IDNCT06846307

SponsorUniversitas Diponegoro

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-01-29

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