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Comparison the analgesic efficacy of intramuscular morphine and morphine suppository in renal colic

Comparison the analgesic efficacy of intramuscular morphine and morphine suppository in patients with renal colic

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015111825098N1
Enrollment
84
Registered
2016-03-18
Start date
2016-02-20
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

renal colic. unspecified renal colic

Interventions

Intervention 1: Intervention group: Patients with renal colic that receive 10 mg intramuscular Morphine Sulfate (manufactured by Darou Pakhsh Pharmaceutical Co.) for control of pain. Intervention 2: C
Treatment - Drugs
Intervention group: Patients with renal colic that receive 10 mg intramuscular Morphine Sulfate (manufactured by Darou Pakhsh Pharmaceutical Co.) for control of pain
Control group: Patients with renal colic that receive 10 mg suppository of Morphine Sulfate (brand name: Opirect, manufactured by Aburaihan Pharmaceutical Co.) for control of pain

Sponsors

Vice Chancellor for research of Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 18-55 years old patients with unilateral acute flank or abdominal colicky pain that in evaluation of the patient with ultrasonography, CT scan or intravenous pyelography presence of the urinary stone is approved or the patient passes the stone. Exclusion criteria : sensitivity to morphine; addiction; fever higher than 38 degrees of centigrade; unstable hemodynamic condition; impaired hepatic or renal function; heart failure; respiratory failure; suspected to peritonitis; pregnancy or suspected to pregnancy; transplanted kidney; suspected to aneurysm or dissection of aorta and receiving analgesic within 6 hours before admission.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before intervention, 15, 30 and 60 minutes after intervention. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Blood pressure. Timepoint: Before intervention, 15, 30 and 60 minutes after intervention. Method of measurement: Sphygmomanometer.;Heart rate. Timepoint: Before intervention, 15, 30 and 60 minutes after intervention. Method of measurement: Counting the number of radial pulse.;Respiratory rate. Timepoint: Before intervention, 15, 30 and 60 minutes after intervention. Method of measurement: Counting the number of breaths.;Nausea and Vomiting. Timepoint: Before intervention, 15, 30 and 60 minutes after intervention. Method of measurement: Question of the patient and observation.;Dizziness. Timepoint: 15, 30 and 60 minutes after intervention. Method of measurement: Question of the patient.;Drowsiness. Timepoint: 15, 30 and 60 minutes after intervention. Method of measurement: Observation.;Facial Flushing. Timepoint: 15, 30 and 60 minutes after intervention. Method of measurement: Observation.;Size of urinary stone. Timepoint: After intervention. Method of measurement: Imaging findings.;Location of the stone. Timepoint: After intervention. Method of measurement: Imaging findings.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Arash Ardestani Zadeh

Semnan University of Medical Sciences

ardestani_a@yahoo.com+98 23 3343 7830

Outcome results

None listed

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