Skip to content

The effect of lidocaine on acute renal colic pain

Effects of adding intravenous lidocaine and morphine on pain of acute renal colic

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201404196803N7
Enrollment
120
Registered
2014-04-24
Start date
2013-04-21
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

Acute renal colic pain. Unspecified renal colic

Interventions

Intervention 1: In the intervention group 1.5 mg/kg IV lidocaine with 0.1 mg/kg IV morphine will be administered. Intervention 2: In the control group 0.1 mg/kg IV morphine with intravenous saline as
Treatment - Drugs
In the intervention group 1.5 mg/kg IV lidocaine with 0.1 mg/kg IV morphine will be administered.
In the control group 0.1 mg/kg IV morphine with intravenous saline as placebo will be administered.

Sponsors

Vice chancellor for research, Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Informed written consent; Clinical signs of renal colic with at least one of the three cases, hematuria in urinalysis, seeing stone in radiography (Kidney Ureter Bladder = KUB) and sonography of the urinary tract. Exclusion criteria: Patient's unwillingness to continue participation in the study at any time; History of cardiac disease, hypertension and asthma; Pregnancy; substance abuse; History of frequent acute renal colic (more than 3 times per year); Sensitivity to lidocaine.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Acute renal colic pain. Timepoint: Before intervention, and at 5, 10, 30, 60 and 120 minutes after the intervention. Method of measurement: Visual Analog Scale.

Secondary

MeasureTime frame
Nausea and vomiting due to acute renal colic. Timepoint: Before intervention, and at 5, 10, 30, 60 and 120 minutes after the intervention. Method of measurement: Visual Analog Scale.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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