Moderate acute pain in the emergency department: Evaluation of the efficacy of oral versus intravenous paracetamol

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202409681111186

Enrollment

300

Registered

2024-09-19

Start date

2024-10-01

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

analgesia

Interventions

group A

group B

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: -Patients aged 18 and over - Any moderate acute pain of traumatic or non-traumatic origin : 4 = VAS <6

Exclusion criteria

Exclusion criteria: - Vomiting within 30 minutes of taking oral paracetamol - Incomplete intake of paracetamol dose - Patient escaped or discharged against medical advice prior to efficacy assessment within 30 min.

Design outcomes

Primary

Measure	Time frame
VAS = 3 at T 30 min	—

Secondary

Measure	Time frame
- Safety: major adverse events (anaphylaxis/hypotension) or minor adverse events (digestive disorders, allergic reaction, injection site complications) ;Use of rescue analgesia: morphine titration	—

Countries

Tunisia

Contacts

Public Contactsarra jouini

emergency department

jouinisarra2007@gmail.com21622510892

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026