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Comparison of the analgesic effect of Magnesium-sulfate and Paracetamol with Paracetamol and Placebo in the treatment of renal colic

Comparison of the analgesic effect of Magnesium-sulfate and Paracetamol with Paracetamol and Placebo in the treatment of renal colic patients: double-blind clinical trial study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190907044717N1
Enrollment
80
Registered
2020-04-08
Start date
2020-04-20
Completion date
Unknown
Last updated
2020-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal colic. Unspecified renal colic

Interventions

Intervention 1: Intervention group: Intravenous Paracetamol 15 mg/ kg single dose plus 100 ml normal saline including magnesium sulfate 50% 15 mg/kg as single dose. Intervention 2: Control group: Intr

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Individuals who are clinically suspected of having renal colic or have been diagnosed with ultrasound or CT scan with a definitive diagnosis of renal colic Minimum score of 5 from the visual analogue scale(VAS) at baseline Glasgow Coma Scale(GCS) of 15

Exclusion criteria

Exclusion criteria: Body temperature > 38° C Pregnancy or any doubt about pregnancy Use of pain medication during the last 6 hours Abdominal pain and the possibility of peritonitis Not signing the informed consent Unstable clinical conditions and hypotension(systolic pressure less than 90 or 20% of baseline pressure) and bradycardia(less than 60) and respiratory rate lower than 16 Disposal of stone(s) History of heart diseases History of liver diseases History of kidney diseases History of metabolic diseases History of seizures Drug history of calcium channel blockers History of alcoholism History of mental disorders, depression and recent use of sedative or anti-psychotic or antidepressants History of drug abuse and addiction History of neuro-muscular disease and underlying bradycardia (heart rate less than 60) and long QRS interval History of hypotension History of hypocalcemia and hypomagnesemia Barbiturates and general anesthetics use

Design outcomes

Primary

MeasureTime frame
The severity of renal colic's pain. Timepoint: Before the intervention and 20, 40, and 60 minutes after the intervention. Method of measurement: Visual Analog Scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParham Torabinavid

Hamedan University of Medical Sciences

parham.salva@gmail.com+98 81 3838 0572

Outcome results

None listed

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