Assessment of mini-dose of suxamethonium effects to facilitate Laryngeal Mask Airway insertion with semi inflated cuff under propofol anesthesia

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201107181772N6

Enrollment

Registered

2011-08-13

Start date

2011-04-09

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

Laryngial mask airway insertion. Fitting and adjustment of other specified devices

Interventions

Intervention 1: After per oxygenation, induction of anesthesia is achieved with Fentanil 1µg/kg, Midazolam, .01mg/kg and Propoful 2mg/kg, then patients are ventilated by face mask, until enough depth

Treatment - Drugs

After per oxygenation, induction of anesthesia is achieved with Fentanil 1µg/kg, Midazolam, .01mg/kg and Propoful 2mg/kg, then patients are ventilated by face mask, until enough depth of anesthesia is

After per oxygenation, induction of anesthesia is achieved with Fentanil 1µg/kg, Midazolam, .01 mg/kg and Propoful 2mg/kg, then Suxamethonium, 0/1mg/kg was added to induction drugs. Then patients are

Eligibility

Sex/Gender

All

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: age 20 to 60 years old, need for cystoscopy, ASA grade 1-2, mallampathy grade 1-2 Exclusion Criteria: Anatomical disorder, drug hypersensitivity, patient’s refusal, addiction, history of atypical plasma colinestrase, artificial teeth, mallampathy score 3-4

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Number of Propofols consumed. Timepoint: During anesthesia. Method of measurement: In milligram.	—

Secondary

Measure	Time frame
Exteremities movement. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Laryngospasm. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Bucking. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Coughing. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Rate of attempt to insertion. Timepoint: during induction of anesthesia. Method of measurement: number of trying.;Myalgia. Timepoint: in recovery period. Method of measurement: scoring from 0 to 10 (VAS).;Head movement. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Difficulty of insertion. Timepoint: after induction of anesthesia. Method of measurement: scoring from 0 to 3.;Sore throat. Timepoint: in recovery period. Method of measurement: scoring from 0 to 10 (VAS).	—

Measure

Time frame

Exteremities movement. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Laryngospasm. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Bucking. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Coughing. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Rate of attempt to insertion. Timepoint: during induction of anesthesia. Method of measurement: number of trying.;Myalgia. Timepoint: in recovery period. Method of measurement: scoring from 0 to 10 (VAS).;Head movement. Timepoint: during anesthesia. Method of measurement: scoring from 0 to 3.;Difficulty of insertion. Timepoint: after induction of anesthesia. Method of measurement: scoring from 0 to 3.;Sore throat. Timepoint: in recovery period. Method of measurement: scoring from 0 to 10 (VAS).

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDawood Aghamohammadi

Anesthesia research team, Tabriz University of Medical Sciences

aghamohammadid@tbzmed.ac.ir daghamohamadi@yahoo.com+98 41 1381 8940

Outcome results

None listed

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