A comparison of sedation with thiopental–fentanyl versus propofol–fentanyl for anterior shoulder dislocation reduction in Emergency department

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210626051714N1

Enrollment

100

Registered

2021-07-16

Start date

2019-09-23

Completion date

Unknown

Last updated

2021-08-30

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

Conditions

Anterior Shoulder Dislocations. Anterior dislocation of unspecified humerus, initial encounter

Interventions

Intervention 1: Intervention group: In group A patients, propofol - 0.5 mg / kg fentanyl µg/kg was used as intervention group A. Intervention 2: Intervention group: In group B, thiopental was used tit

Eligibility

Sex/Gender

All

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the study People 18 to 40 years old with anterior shoulder dislocation

Exclusion criteria

Exclusion criteria: Patients with fractures and major dislocations Other major injuries with hemodynamic disturbances History of substance abuse Patients with allergies to any of the drugs Pregnancy

Design outcomes

Primary

Measure	Time frame
Duration of sedation in three stages 1- Start of sedation 2- Between sedation and awakening 3- Between awakening to full consciousness. Timepoint: 1- Start of sedation 2- Between sedation and awakening 3- Between awakening to full consciousness. Method of measurement: Using a stopwatch.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Nayereh Garjani

Zanjan University of Medical Sciences

ngarjani@zums.ac.ir009833130000

Outcome results

None listed

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