Double J stent removal. Calculus of kidney and ureter
Conditions
Interventions
Intervention 1: Intervention group1 : In the propofol( B.BRAUN company) group, 150 mg per 15 cc syringe is infused with a loading dose of 0.1 mg / kg and a maintenance dose of 0.3-0.5 mg / kg / hour,
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: One sided double J Age older than18 years
Exclusion criteria
Exclusion criteria: Lack of history of chronic use of sedatives, alcohol and drugs Lack of history of chronic use of sedatives, alcohol and drugs Lack of mental disorders and difficulty communicating Absence of renal failure (serum creatinin> 1.5 mg / dL). Absence of acute upper respiratory tract infection Absence of chronic pain syndrome in patients Lack of sensitivity to study's drugs Absence of prostatitis or urethral stricture during cystoscopy. Absence of lower urinary tract symptoms before the start of the procedure.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of sedation. Timepoint: Calculate the duration of sedation from the start of surgery to the time of recovery consciousness. Method of measurement: Based on sedation hours.;Sedation degree. Timepoint: Record the degree of sedation during surgery. Method of measurement: Ramsey questionnaire.;Additional dose of sedative. Timepoint: The amount of additional drug injected is calculated after the end of surgery. Method of measurement: Questionnaire.;Nausea, vomiting, chills, anxiety and apnea due to sedatives. Timepoint: Complications will be recorded during surgery and recovery. Method of measurement: Questionnaire.;The effect of sedatives on blood pressure, heart rate and O2 saturation. Timepoint: Vital signs before surgery are recorded every 5 minutes during surgery and every 10 minutes during the stay in recovery. Method of measurement: Pressure is recorded by a mercury sphygmomanometer and pulse and blood oxygen are recorded by pulse oximeter.;Patient satisfaction. Timepoint: After exiting the recovery. Method of measurement: Satisfaction according to Likert scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFaride Akrami Moghaddam
Esfahan University of Medical Sciences
Outcome results
None listed