Comparison of the three drug combination succinylcholine and thiopental "with" propofol and fentanyl "or" intravenous midazolam and fentanyl "success and complication reduction in shoulder

The comparison of the success and complications in shoulders reduction with using three drug combination succinylcholine and thiopental "with" propofol and fentanyl "with" midazolam and fentanyl in Imam Hussein hospital of Tehran.

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017032323559N10

Enrollment

150

Registered

2017-04-24

Start date

2017-04-21

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

Reduction of shoulders. Dislocation of shoulder joint

Interventions

Intervention 1: The first group: consists of succinylcholine 20 mg and thiopental with 5.3 mg/kg dose(drugs prescription to titrated and slow injection). Intervention 2: The Second group: consists of

Treatment - Drugs

The first group: consists of succinylcholine 20 mg and thiopental with 5.3 mg/kg dose(drugs prescription to titrated and slow injection)

The Second group: consists of propofol with 1-3 mg/kg doses and Fentanyl with 2-3 mg/kg dose(drugs prescription to titrated and slow injection)

The third group: includes a midazolam with 3-5 mg dose and fentanyl with 2-3 mg/kg dose(drugs prescription to titrated and slow injection)

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients 18 to 65 years old with anterior or posterior shoulder dislocation; Admitted to the emergency; consent to participate in the study. Exclusion criteria: physical condition above III based on the ASA; patients with major fracture dislocation; other major injuries; history of drug abuse; patients with poisoning.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Reduction success. Timepoint: Up to 5 minutes after reduction. Method of measurement: Checked by X-ray.;Reduction complications. Timepoint: Until clearance. Method of measurement: Through examination of patient.	—

Secondary

Measure	Time frame
Pain score. Timepoint: During reduction. Method of measurement: Based on VAS score.;Sedation score. Timepoint: During reduction. Method of measurement: Ramsey sedation score.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid kariman MD

shahid Beheshti University of Medical Sciences

h.kariman49@gmail.com+98 21 7755 8001

Outcome results

None listed

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