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Adding Dexmedetomidine to Mannitol to Attenuate the Increase of Intracranial Pressure

Adding Dexmedetomidine to Mannitol to Attenuate the Increase of Intracranial Pressure

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07064720
Enrollment
60
Registered
2025-07-15
Start date
2024-07-12
Completion date
2026-01-15
Last updated
2026-01-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dexmedetomidine

Keywords

dexmedetomidine, mannitol

Brief summary

Dexmedetomidine is a potent alpha-2 adrenergic receptor agonist. In addition, dexmedetomidine-induced stimulation of the postsynaptic alpha-2 adrenergic receptor on the cerebral blood vessels can cause cerebral vasoconstriction and decrease cerebral blood flow

Interventions

DRUGDexmedetomidine with Mannitol

receive 1 mcg/kg of dexmedetomidine added to 0.4 mcg/kg of mannitol

receive 0.5 g/kg of mannitol

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

ASA I-II Patients scheduled for elective robot-assisted laparoscopic prostatectomy

Exclusion criteria

* • ASA physical status \> II * Cardiac patients * Cerebrovascular disease * Glaucoma * Hepatic failure * Renal failure * History of anaphylactic reaction to dexmedetomidine or mannitol * Hemodynamic instability * Cannot measure ONSD for example due to ophthalmological problems. * Any cause of preoperative increase in ICP for example intracranial space occupying lesions.

Design outcomes

Primary

MeasureTime frame
optic nerve sheath diameter90 minutes

Secondary

MeasureTime frame
Postoperative neurologic complications24 HOURS
Postoperative cardiac complications24 hours
Duration of hospital stay30 days

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026