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study of the analgesic effect of fentanyl, fentanyl with ibuprofen, fentanyl with apotel and fentanyl with ketorolac in patients with renal colic

Phase 2
Recruiting
Conditions
Renal colic.
Unspecified renal colic
Registration Number
IRCT20220421054605N1
Lead Sponsor
Shahre-kord University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

Patients over the age of 18
have renal colic
have stable hemodynamics(pulse rate(PR)=60-100,systolic blood pressure(SBP)>100,respiratory rate(RR)=8-22,functional oxygen saturation(SPO2)>90%)
Have informed consent to participate in this study
Don't have any of the following: Pregnancy/Asthma / chronic obstructive pulmonary disease(COPD)/ Intestinal obstruction/ Hypertension and heart failure/ Previous pulmonary surgery of the kidney and urinary tract/ Peptic ulcer/ Gastrointestinal bleeding/ Previous allergies to fentanyl or other analgesics / Loss of consciousness/ Trauma Head and chest/pneumocephalus/pneumothorax/Drug addiction/tenderness and abdominal rebound/Guarding abdomen/menstruation retarded/Use of analgesics in the past 24 hours
No liver failure and bilateral renal failure

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score. Timepoint: At the beginning of the study and at 5, 10? 15? 20? 25 and 30 minutes after the intervention. Method of measurement: Visual Analogue Scale (VAS).
Secondary Outcome Measures
NameTimeMethod
Mean Arterial Pressure. Timepoint: At the beginning of the study and at 5, 10? 15? 20? 25 and 30 minutes after the intervention. Method of measurement: Monitoring device.;Hear rate. Timepoint: At the beginning of the study and at 5, 10? 15? 20? 25 and 30 minutes after the intervention. Method of measurement: Monitoring device.;Percentage of blood oxygen. Timepoint: At the beginning of the study and at 5, 10? 15? 20? 25 and 30 minutes after the intervention. Method of measurement: Monitoring device.
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