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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03722940
Other study ID # Bahtem WBAKHET
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date June 1, 2014
Est. completion date August 1, 2018

Study information

Verified date October 2019
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine the efficiency of addition of magnesium sulfate to total intravenous anesthesia (TIVA) in optimizing the surgical field during pediatric cochlear implant surgery. Also its effects on the intraoperative evoked stapedial reflex thresholds (ESRT) and the intraoperative anesthetic requirements were evaluated.


Description:

Sixty-six ASA I and II children (1-6 years) undergoing cochlear implantation under general anesthesia were enrolled in this double blind, randomized study. Children were randomly allocated into two equal groups. Children in Group M (magnesium sulphate group) received an iv bolus dose of magnesium sulfate 40 mg Kg-1 over 5 minutes before induction of anesthesia followed by 15mg Kg-1 h-1 infusion until the start of skin closure. Children in Group C (Control group) received equivalent volumes of isotonic saline solution over the same period instead of magnesium sulphate. Haemodynamic variables, quality of surgical field, ESRT and the intraoperative anesthetic requirements were recorded


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date August 1, 2018
Est. primary completion date May 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- ASA I and II children

Exclusion Criteria:

- uncontrolled hypertension,

- diabetes mellitus,

- liver disease,

- kidney disease,

- heart disease,

- allergy to magnesium sulphate,

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Magnesium sulphate
Before induction of anesthesia; children in group M received an iv bolus dose of magnesium sulfate (Magnesium sulfate ampoule 1 gm/10 ml, Eipico, Egypt) 40 mg Kg-1 over 5 minutes followed by 15 mg Kg-1 h-1 ivi until the start of skin closure.
Other:
Na CL 0.9%
Before induction of anesthesia; children in group C equivalent volumes of Na Cl 0.9% over the same period instead of magnesium sulphate.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Wahba bakhet bahteem specialized hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of surgical field using Fromme's-Boezaart scale (0 to 5). A score of = 2 was considered to be optimal at the end of the surgey
Secondary The operative time Minutes Intraoperative
Secondary The anesthesia time. Minutes Intraoperative
Secondary ESRT responses the surgeon assessed ESRT response at the basal, middle, and apical areas of the electrode array by visual monitoring of the stapedius muscle using direct microscopic examination After insertion of the electrode and after reversal of any residual muscle relaxant (TOF response > 0.9),
Secondary Heart rate beats per minute baseline, after surgical incision, Hypotensive period, after LMA removal and at recovery room admission.
Secondary Mean arterial blood pressure mm Hg Intraoperative
Secondary Anesthetic consumption propofol and fentanyl requirement after the bolus Intraoperative
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