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MgSO4 Combined With Rocuronium Priming

MgSO4 Combined With Rocuronium Priming

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01389791
Enrollment
100
Registered
2011-07-08
Start date
2011-05-31
Completion date
2012-01-31
Last updated
2012-01-10

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

Conditions

Muscle Relaxation

Keywords

muscle relaxation, magnesium sulfate, rocuronium

Brief summary

Priming with either rocuronium or MgSO4 is known to accelerate the effect of rocuronium on muscle relaxation. The purpose of this study is to define the effect of MgSO4 on the rocuronium-priming.

Detailed description

Acceleration of muscle relaxation is beneficial in rapid-sequence intubation. If MgSO4 combined with priming is efficient in accelerating muscle relaxation, it would be an interesting alternative to rapid-sequence intubation.

Interventions

DRUGmagnesium sulfate

Patients in this group receive intravenous MgSO4 50mg/kg before administration of rocuronium (induction dose).

Patients in this group receive 0.06mg/kg of rocuronium before administration of 0.54mg/kg of rocuronium.

DRUGmagnesium sulfate and priming

Patients in this group receive MgSO4 50mg/kg and 0.06mg/kg of rocuronium before administration of 0.54mg/kg of rocuronium.

Sponsors

Seoul National University Bundang Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* patients of ASA Ⅰ-Ⅱ * aged 18\ 65 * scheduled to undergo elective surgery under general anesthesia

Exclusion criteria

* risk of pulmonary aspiration * anticipated airway difficulty * reactive airway disease * allergic to study drugs * neuromuscular / cardiovascular/ renal/ hepatic disease * atrioventricular conduction disturbance * BMI \< 18.5 or \> 24.9 * chronic treatment with calcium channel blocker * medications which affect muscle relaxation

Design outcomes

Primary

MeasureTime frame
time from injection of induction dose of rocuronium until 95% depression of TOFtime from injection of induction dose of rocuronium until 95% depression of TOF, upto 5 min

Secondary

MeasureTime frameDescription
rocuronium durationtime from injection of induction dose of rocuronium until train-of-four count reaches two.time from injection of induction dose of rocuronium until train-of-four count reaches two.
intubating conditiontime from injection of induction dose of rocuronium until tracheal intubation.rapid sesequence intubation condition is evaluated.

Countries

South Korea

Contacts

Primary ContactMihyun Kim, MD
snmd56@yahoo.com82-31-787-2034

Outcome results

None listed

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