ClinicalTrials.Veeva

Menu

The Therapeutic Time Window of Mannitol During Craniotomy for Optimal Brain Relaxation in Patients With Supratentorial Tumours

Fudan University logo

Fudan University

Status

Completed

Conditions

Supratentorial Tumors

Treatments

Drug: Mannitol

Study type

Interventional

Funder types

Other

Identifiers

NCT03444519
KY2017-306

Details and patient eligibility

About

Although mannitol is used for brain relaxation during neurosurgery and in the treatment of raised intracranial pressure; there is not a consensus on its safe, effective dose and the duration of its administration. This study aimed to compare the effects of the mannitol in different use times, on the brain relaxation, electrolyte, lactate levels of the blood, peroperative fluid balance and the volume of the urine in supratentorial mass resection surgeries.

Enrollment

100 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Intracranial shift >3mm
  • Scheduled for supratentorial mass resection under elective conditions

Exclusion criteria

  • Decompensated heart failure
  • kidney insufficiency
  • Diabetes insipidus,
  • Electrolyte imbalance and
  • Who are unconscious

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 2 patient groups

Mannitol A
Experimental group
Description:
in this group, Mannitol (1.0g/kg) is given just after the induction of general anesthesia
Treatment:
Drug: Mannitol
Mannitol B
Active Comparator group
Description:
in this group, Mannitol (1.0g/kg) is given at the time of skin incision
Treatment:
Drug: Mannitol

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems