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Clinical Trial Summary

compare the operating condition of two different levels of muscle relaxation on facial nerve monitoring using transcranial motor evocked potential in CPA surgery . - To Estimate End to start facial nerve MEP amplitude ratio - To determine the effect of neuromuscular relaxant degrees on recovery and - Assessment of propofol doses needed for enhancement of early recovery and ambulation.


Clinical Trial Description

40 Patients aged from 18-60 years old undergoing Cerebellopontine angle surgery. Patients will be one of two groups: Both Induction will be accomplished with fentanyl, propofol , rocronium infusion will be given randomly to one of the groups. Depth of anaesthesia, neurotransmitter monitoring and facial nerve neurophysiological monitoring will be done. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04148534
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date November 1, 2019
Completion date November 15, 2020

See also
  Status Clinical Trial Phase
Recruiting NCT04249921 - Evaluation of Acupuncture Effects for Complications After Surgery of Cerebellopontine Angle Tumor in Skull Base
Not yet recruiting NCT03228511 - Endoscopic-assisted Microsurgical Removal of Cerebellopontine Angle Lesions N/A