Comparison of oxycodone and naproxen in pain control of acute soft tissue injuries

Comparison of oxycodone and naproxen in pain control of soft tissue injuries

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT201112208104N3

Enrollment

150

Registered

2012-08-31

Start date

2012-01-01

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

soft tissue injuries. musculoskeletal system and connective tissue

Interventions

Intervention 1: First group will receive 250 mg Naproxen. Intervention 2: Second group receive 10 mg Oxycodone.

Treatment - Drugs

First group will receive 250 mg Naproxen

Second group receive 10 mg Oxycodone

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criterion: patients above 18 years old with soft tissue injuries. Exclusion criteria: contraindications for opioids and NSAIDs and presence of fracture.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain control. Timepoint: 0, 30, 60 minutes after treatment. Method of measurement: Numeric Rating Scale.	—

Secondary

Measure	Time frame
Presence of side effects. Timepoint: 30 and 60 minutes after treatment. Method of measurement: Patient monitoring.;Need for follow up analgesic. Timepoint: First 24 hours after discharge. Method of measurement: Telephone follow up.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Amin Zare

Tehran University of Medical Sciences

mazare74@yahoo.com+98 21 6652 5327

Outcome results

None listed

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