Skip to content

Evaluation of the effect of Ketamine by nebulizer in reducing pain caused by renal colic.

Comparison of the analgesic effect of nebulized Ketamine versus intravenous Ketorolac in reducing pain of patients with renal colic who refer to emergency department

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220201053906N1
Enrollment
108
Registered
2022-06-05
Start date
2022-05-22
Completion date
Unknown
Last updated
2022-06-27

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: The nurse nebulizes 0.5 mg/kg Ketamine and injects 1 cc / kg normal saline For the patient who is a member of the intervention group. Intervention 2: Control group

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients 20-70 years old With acute pain in one side flank Has informed consent

Exclusion criteria

Exclusion criteria: Unstable patients ( SBP100 or HR<60, fever) Pregnant or Suspicion of pregnancy Single kidney Hasn't informed consent or unable to have informed consent Want to discharge before ending the study(2 hours after starting the study) History of addiction History of take analgesic at least 6 hours Symptom or sign of acute abdominal (tenderness, guarding, rebound) Need Rescue dose before ending of the study

Design outcomes

Primary

MeasureTime frame
Score of renal colic pain in NRS. Timepoint: Before starting the study, 5, 15, 30 and 60 minutes after starting the study. Method of measurement: Numeric rating scale (NRS).

Secondary

MeasureTime frame
Patient satisfaction with pain control. Timepoint: 2 hours after the start of the study. Method of measurement: Asking verbal.;Side effects of the treatments. Timepoint: Before starting the study, 5, 15, 30, 60 minutes after starting the study and if the patient has been in the hospital for more than 2 hours; At the time of discharge of the patient. Method of measurement: Medical history and physical examination.;Duration of the patient's presence in the emergency department. Timepoint: At the time of discharge of the patient. Method of measurement: Clock.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactYasaman Safari

Shahroud University of Medical Sciences

asemon.violet@gmail.com0098 21 2231020

Outcome results

None listed

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