Skip to content

Comparison the rate of trauma, ease of placement and hemodynamic changes following placement of Laryngeal Mask Airway with or without the use of muscle relaxants in patients undergoing elective surgery

Comparison the respiratory complications of Laryngeal Mask Airway insertion with or without the use of muscle relaxants in patients undergoing elective surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201305081766N6
Enrollment
60
Registered
2015-02-15
Start date
2013-04-04
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Airway managment using laryngeal mask airway. Skeletal muscle relaxants [neuromuscular blocking agents]

Interventions

Intervention 1: Intervention group: after placement of standard monitors and in the beginning of anesthesia, 0.15 mg/kg atracurium (that volume of that reached to 2ml with adding normal saline) will b
Treatment - Drugs
Placebo
Intervention group: after placement of standard monitors and in the beginning of anesthesia, 0.15 mg/kg atracurium (that volume of that reached to 2ml with adding normal saline) will be injected intra
Control group: after placement of standard monitors, and in the beginning of anesthesia, 2ml normal saline will be injected intravenously, that followed by other anesthetic agents.

Sponsors

Vice chancellor for research, Kurdistan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criterion : ASA physical status 1 or 2. Exclusion criteria : ASA physical status 3 or more; pregnancy; history of gastro oesophageal reflux, hiatal hernia; history of mouscloskletal disease; history of allergy to muscle relaxants; needs to endotracheal intubation during anesthesia and history of drug or alcohol abuse.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Time of LMA insertion. Timepoint: Once. Method of measurement: The time from mouth opening to proof chest expantion with compresion of anesthesia bag.

Secondary

MeasureTime frame
Ease of LMA insertion. Timepoint: once. Method of measurement: Straightforward = completion of insertion in first attempt in less than 15 second, and without displacement. Slightly difficult = completion of insertion in first attempt in more than 15 second, and with displacement. Difficult = completion of insertion needs more than one attempt, in more than 30 second ,and with multiple displacements .;Patients' response to LMA insertion. Timepoint: Once , for two minute in the beginning of anesthesia , and after insertion of LMA and insufflation of that cuffs. Method of measurement: Yes = movement of limbs, coughing, straining,resistance against manually ventilation , and keeping breathing. No = absence of the aforementioned conditions.;Air leak from the LMA environment. Timepoint: Once. Method of measurement: Yes= Audible sound in the time of mandatory ventilation . NO= Loss of sound in the time of mandatory ventilation.;The number of attempts to insertion of LMA. Timepoint: Once. Method of measurement: The number of times that the LMA imported from the outside the mouth to verify its accuracy of insertion , and the number will be written.;The quality of pulmonary ventilation. Timepoint: Once. Method of measurement: Good = good chest expansion, lack of audible air leaks, lack of gastric distention, and square wave in Capnography.Bad = lack of previous conditions.;Recovery time. Timepoint: Once. Method of measurement: The time between discontinuation of drugs to elevating of head for 10 minutes.;Cardiovascular profile. Timepoint: before injection of anesthetic drugs , after injection of anesthetic drugs , after insertion of LMA , every 15 minutes tell recovery from anesthesia. Method of measurement: By automated monitor ( sadat co. Iran).;Complications during removal of LMA. Timepoint: After removal of LMA, until exit of patient from post-anesthesia care unit. Method of measurement: with the patient monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKarim Nasseri

Kurdistan University of medical Sciences

nasseri_k@muk.ac.ir+98 87 1328 2002

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026