Procedural sedation and analgesia of reduction of shoulder dislocation.

A clinical trial to compare the effectiveness of ketamine, propofol/ketamin with propofol/fentanilel for procedure sedation and analgesia of reduction of shoulder dislocation.

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180627040258N1

Enrollment

150

Registered

2018-07-11

Start date

2018-09-01

Completion date

Unknown

Last updated

2018-09-11

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

Conditions

Dislocation of shoulder joint. Subluxation and dislocation of shoulder joint

Interventions

Intervention 1: Intervention group I: patients are revising 1-1.5 mg/kg of intravenous ketamine from 30 to 60 seconds. Intervention 2: Intervention group II: patients are revising 1-1.5 mg/kg of intra

Eligibility

Sex/Gender

All

Age

15 Years to 40 Years

Inclusion criteria

Inclusion criteria: Aged between 15 and 40 years Lake of underlying disease such as blood pressure, diabetic, cardiovascular disease, and etc Having dislocation orthopedic removable at emergency Normal examination of the neuromuscular system Non allergenic to sedative drug

Exclusion criteria

Exclusion criteria: Cardiovascular instability Having low saccharification Having multiple trauma Possibility of the abdomen or chest bleeding Having head trauma Decreased alertness

Design outcomes

Primary

Measure	Time frame
Rate of pain. Timepoint: before and per minute until the completed reduction. Method of measurement: bispectral index scale (BIS).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasood Shahabian

Artesh University of Medical Sciences

elmpajooh@yahoo.com+98 21 3321 6512

Outcome results

None listed

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