Opioid induced cough. Whooping cough, unspecified
Conditions
Interventions
Intervention 1: Intervention group 1: Fentanyl will be prepared in 5 cc syringes randomly injected. Intervention 2: Intervention group 2: lidocaine will be prepared in 5 cc syringes and after closing
Treatment - Drugs
Placebo
Intervention group 1: Fentanyl will be prepared in 5 cc syringes randomly injected.
Intervention group 2: lidocaine will be prepared in 5 cc syringes and after closing cord randomly injected.
Sponsors
Urmia University of Medical Sciences
Vice Chancellor for research of Urmia University of Medical Sciences
Eligibility
Sex/Gender
All
Age
2 Years to 10 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria:Anesthesiologists physical status I ,II; aged 2 to10 years old; elective hernioraphy; general anesthesia Exclusion criteria: patients with body weight less than 20% of the ideal body weight; emergency hernioraphy; a history of asthma; chronic obstructive lung diseases; chronic cough; upper respiratory tract infection within 4 weeks of Surgery; children with malformation of the tongue and oropharynx; allergy to the study drugs
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cough. Timepoint: Within 2 minutes after fentanyl injection. Method of measurement: patient observation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Mean Arterial Blood Pressure. Timepoint: Within 2 minutes after fentanyl injection. Method of measurement: None Invasive Blood Pressure.;Pulse rate. Timepoint: Within 2 minutes after fentanyl injection. Method of measurement: Electrocardiogram.;The percentage of arterial oxygen. Timepoint: Within 2 minutes after fentanyl injection. Method of measurement: Pulse Oximetry. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShahryar Sane
Vice chancellor for research, Urmia University of Medical Sciences
Outcome results
None listed