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Desmopressin in the treatment of renal colic

Phase 3
Recruiting
Conditions
Renal colic.
Unspecified renal colic
Registration Number
IRCT20180129038549N12
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
135
Inclusion Criteria

Adult patients referred to the emergency department
Known patient with renal colic or typical renal colic pain
Severe pain (VAS> 5)
Age less than 65 years
Informed consent to participate in the study

Exclusion Criteria

History of hypertension
Patients with heart failure, liver and kidney failure
History of analgesic use within 6 hours before the admission
History of drug addiction
Pregnant patients
Patients with decreased level of consciousness
Patients with unstable vital signs
Hypersensitivity to desmopressin, ketamine and morphine

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The severity of pain. Timepoint: In 10, 30 and 60 minutes after receiving the drug. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
Side effects. Timepoint: every 10 minutes. Method of measurement: Physical exam.;Vital signs (blood oxygen saturation level, pulse rate and respiratory rate per minute). Timepoint: Every 10 minutes. Method of measurement: Physical exam.
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