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Comparison of Ketamin/Propofol (Ketofol) and Etomidate /Fentanyl (Etofen) in reduction of shoulder dislocation

Comparison of Ketamin/Propofol (Ketofol) and Etomidate /Fentanyl (Etofen) combinations for procedural sedation and analgesia of anterior shoulder dislocation reduction in Emergency Department: A Randomized Clinical Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220824055790N1
Enrollment
46
Registered
2022-09-13
Start date
2022-10-23
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Anterior Shoulder Dislocation. Subluxation and dislocation of shoulder joint

Interventions

Intervention 1: Intervention group: According to the PSAs protocol, Ketofol with a dose of 0.75 mg/kg IV bolus of ketamine and propofol are given as starting doses. A repeat dose of 0.375 mg/kg ketami

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Adults between 18 and 50 years old Anterior shoulder dislocation

Exclusion criteria

Exclusion criteria: History of allergy to any of the drugs (ketamine, propofol, etomidate, fentanyl) underlying cardiovascular disease lung diseases nervous system diseases (central or peripheral) history of current drug or stimulant abuse now or in the last month associated fracture neurovascular symptoms patient dissatisfaction associated diseases

Design outcomes

Primary

MeasureTime frame
Pain score: using numerical rating scale. Timepoint: During Reduction. Method of measurement: Ask the patient: Score from 1 to 10.;Number of reduction attempts until reduction succeeds. Timepoint: During study until reduction succeeds. Method of measurement: -.;Length of stay in the emergency room: the time between the patient's admission to the emergency room and discharge. Timepoint: After discharge. Method of measurement: View the patient file.;Drug side effects: bradycardia, respiratory depression, hypotension. Timepoint: During Study. Method of measurement: Based on the form of drug side effects.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Mojtaba Habibi Khorasani

Kerman University of Medical Sciences

mojista.1375@gmail.com+98 34 3223 5011

Outcome results

None listed

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