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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02502032
Other study ID # ZZ0716
Secondary ID
Status Completed
Phase Phase 3
First received July 16, 2015
Last updated October 8, 2015
Start date July 2015
Est. completion date October 2015

Study information

Verified date October 2015
Source Yangzhou No.1 People's Hospital
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Interventional

Clinical Trial Summary

To investigate the effects of different doses of cisatracurium pretreatment on succinylcholine-induced fasciculations.


Description:

Ninety patients scheduled for laparoscopic cholecystectomies were equally randomized into three groups to receive pretreatment of 0.005, 0.01, and 0.02 mg/kg cisatracurium, respectively. General anesthesia was induced 3.5 min later, train of four stimulation was monitored 4.5 min later, succinylcholine 1.5 mg/kg was injected 5 min later, and endotracheal intubation was implemented 6.5 min later. The side effects of cisatracurium, intensity of fasciculations, intubating conditions, time and extent to maximal depression of twitch and time for its recovery to 20% of control value, severity of myalgia at 24 h postoperatively, serum potassium before cisatracurium pretreatments, at intubating time, and 5 min after intubation were recorded.


Recruitment information / eligibility

Status Completed
Enrollment 87
Est. completion date October 2015
Est. primary completion date October 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria:

- American Standards Association (ASA) physical status I or II patients scheduled for elective laparoscopic cholecystectomies with tracheal intubation requiring general anesthesia;

- 20 - 65 years old;

- Without acid-base imbalance and electrolyte disturbance;

- With normal hepatic and renal function.

Exclusion Criteria:

- Patients with the contraindications associated with succinylcholine or cisatracurium;

- Patients taking drugs known to alter the action of neuromuscular blockers;

- Patients with a body mass index exceeding 30

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Drug:
Cisatracurium
Different groups received different pretreatments of cisatracurium.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Zhuan Zhang

Outcome

Type Measure Description Time frame Safety issue
Primary Presence of fasciculations After the injection of succinylcholine for 1.5 minutes Yes
Secondary Side effects of the pretreatment of cisatracurium From the time of 3 minutes after the pretreatment of cisatracurium for 0.5 minutes Yes
Secondary The time to maximal depression of twitch From the time of 4.5 minutes after the pretreatment of cisatracurium for two minutes Yes
Secondary The extent to maximal depression of twitch From the time of 4.5 minutes after the pretreatment of cisatracurium for two minutes Yes
Secondary The grades of endotracheal intubation At intubating time Yes
Secondary The changes of serum potassium After entering the operating theater till the anesthesia induction, at intubating, and 5 min after intubation Yes
Secondary Myalgia at 24 hours postoperatively At 24 hours postoperatively Yes
See also
  Status Clinical Trial Phase
Completed NCT01902641 - Muscle Relaxation for Short Procedures N/A