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Compare the Operating Condition of Two Levels of Muscle Relaxation on Facial Nerve MEP Monitoring in CPA Surgery

M

Muhammad Magdy Gaber

Status

Completed

Conditions

Cerebellopontine Angle Tumor

Treatments

Drug: Rocroniom, Non Depolarizing Muscle Relaxant

Study type

Interventional

Funder types

Other

Identifiers

NCT04148534
D-4-2019

Details and patient eligibility

About

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.

Full 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.

Enrollment

40 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients age between >18 and<60.
  • Patients scheduled for neurosurgical CPA surgeries
  • Ability to sign the consent
  • ASA classification I, II

Exclusion criteria

  • ASA > II
  • Hemodynamically unstable
  • Disease affecting neuromuscular transmission (myasthenia gravies ...etc.)
  • GCS < 15.
  • Any cardiac patient (ischemic heart disease - cardiomyopathy...etc.)

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

40 participants in 2 patient groups, including a placebo group

muscle relaxant
Active Comparator group
Description:
patient who will receive muscle relaxant, patients will receive rocronium infusion by (5 mcg/kg/min) , maintain partial NMB TOF count 2 and targeting BIS = (40-60)
Treatment:
Drug: Rocroniom, Non Depolarizing Muscle Relaxant
without muscle relaxant
Placebo Comparator group
Description:
patient who will not receive muscle relaxant, will recieve normal saline targeting BIS = 40-60.
Treatment:
Drug: Rocroniom, Non Depolarizing Muscle Relaxant

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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