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Magnesium Sulfate Effects on Onset and Duration of Low Dose Rocuronium in Patients Undergoing Laparoscopic Cholecystectomy

Effects of Magnesium Sulfate on Onset and Duration of Low Dose Rocuronium in Patients Undergoing Laparoscopic Cholecystectomy

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02669368
Enrollment
75
Registered
2016-02-01
Start date
2015-03-31
Completion date
Unknown
Last updated
2016-02-01

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

Conditions

Muscle Relaxation

Brief summary

This study aims to evaluate effects of magnesium sulfate on onset and duration of low dose rocuronium, intubation condition and surgical condition in patients undergoing laparoscopic cholecystectomy.

Interventions

DRUGMagnesium Sulfate

Patients in each group receive Magnesium sulfate 30 mg/kg in 0.9% normal saline (total volume 100 ml) intravenously for 5 min before induction of anesthesia

DRUGSaline

Patients in each group receive 0.9% normal saline (total volume 100 ml) alone intravenously for 5 min before induction of anesthesia

DRUGStandard dose Rocuronium

0.6 mg/kg of Rocuronium given with induction of anesthesia

DRUGLow dose Rocuronium

0.45 mg/kg of Rocuronium given with induction of anesthesia

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* American Society of Anesthesiologists physical status 1 or 2. * BMI of 25-34.9 kg/m2. * Patients scheduled for laparoscopic cholecystectomy.

Exclusion criteria

* Severe respiratory or cardiac disease. * Hepatic or renal function impairment. * Neuromuscular disease. * Patients on medications affecting neuromuscular function. * Patients with known allergy to the drugs.

Design outcomes

Primary

MeasureTime frameDescription
The time of onset the action of RocuroniumTime from injection of Rocuronium till T1 suppression more than 95% up to 10 minutes.by using the TOF watch nerve stimulator
The time at which Maximal suppressionTime from the injection of Rocuronium to T1 maximal suppression time (TOF=0) up to an hour.by using the TOF watch nerve stimulator
Reversal of RocuroniumTime from injection of Rocuronium till reversal of T1 (TOF=25%) around an hour after induction of anesthesiaby using the TOF watch nerve stimulator

Secondary

MeasureTime frameDescription
Intubation conditionWithin 10 minutes after induction of anesthesiato score intubation condition on the basis of 6 items: Jaw relaxation, laryngoscopy, vocal cord position, moving of limbs, coughing & change in heart rate.
Surgical conditionDuring surgeryto score a surgical condition according to 7 point likert scale

Countries

Egypt

Outcome results

None listed

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