A blinded randomised controlled trial to assess rapidity, effectiveness, acceptability and safety with intranasal diamorphine compared to oral morphine of analgesia

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN34432067

Enrollment

300

Registered

2003-09-12

Start date

2002-03-01

Completion date

Unknown

Last updated

2015-01-13

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

Conditions

Signs and Symptoms: Pain Signs and Symptoms Pain

Interventions

Intranasal diamorphine vs oral morphine

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Children aged 4-16 years attending the Accident and Emergency (A&E) department 2. With an acute injury who do not need resuscitation 3. Who would normally be offered oral morphine for analgesia

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

Measure	Time frame
Time to onset of analgesia and efficacy of analgesia.	—

Secondary

Measure	Time frame
Not provided at time of registration	—

Countries

United Kingdom

Outcome results

None listed

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