Comparison of the use of lubricant gel and lidocaine gel in the placement of laryngeal mask on Hemodynamic and reactions in the patients out of anesthesia in 501 Army hospital

Comparison of the use of lubricant gel and lidocaine gel during the placement of LAM (Laryngeal Mask Airway) on hemodynamics and symptoms of withdrawal reactions in the patients out of anesthesia in 501 Army hospital

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016011716906N2

Enrollment

Registered

2016-05-11

Start date

2013-03-21

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

Varicocele. Varicocele

Interventions

Intervention 1: Intervention group The use of lidocaine gel during insertion of laryngeal mask the extent one inch or 2.5 cm. Intervention 2: control group The use of lubricant gel during insertion of

Treatment - Drugs

Intervention group The use of lidocaine gel during insertion of laryngeal mask the extent one inch or 2.5 cm

control group The use of lubricant gel during insertion of laryngeal mask the extent one inch or 2.5 cm

Eligibility

Sex/Gender

Male

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Male patients, aged 20 to 60 years; ASA I; varicocelectomy with general anesthesia; completing consciously the consent form to participate in research projects. Exclusion criteria: Over 60 years old; ASA class II ,III and IV; a history of sore throat and lung disease; drug addiction; any heart disease - liver -Kidney; allergic to any medicine.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Blood pressure. Timepoint: evry 5 minutes, before, in during and after itervention. Method of measurement: By using blood pressure measuring equipment.;Heart beat. Timepoint: evry 2 minutes. before, in during and after intervention. Method of measurement: By using ECG monitoring.;Weight. Timepoint: after intervention. Method of measurement: Based on individual weighing with standard scales.;Nauesa and vomiting. Timepoint: before, in during and after intervention. Method of measurement: View raising or attempting to raise involuntary stomach contents.;Sore throat. Timepoint: befor and after intervention. Method of measurement: ask the patient.;Cough. Timepoint: before and after intervention. Method of measurement: observation.;Age. Timepoint: before intervention. Method of measurement: By date of birth (birth certificate).	—

Measure

Time frame

Blood pressure. Timepoint: evry 5 minutes, before, in during and after itervention. Method of measurement: By using blood pressure measuring equipment.;Heart beat. Timepoint: evry 2 minutes. before, in during and after intervention. Method of measurement: By using ECG monitoring.;Weight. Timepoint: after intervention. Method of measurement: Based on individual weighing with standard scales.;Nauesa and vomiting. Timepoint: before, in during and after intervention. Method of measurement: View raising or attempting to raise involuntary stomach contents.;Sore throat. Timepoint: befor and after intervention. Method of measurement: ask the patient.;Cough. Timepoint: before and after intervention. Method of measurement: observation.;Age. Timepoint: before intervention. Method of measurement: By date of birth (birth certificate).

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehzad Kazemi Haki

Urmia University of Medical Sciences

behzad_emt@yahoo.com+98 44 4222 5779

Outcome results

None listed

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