Does a pain pump provide increased analgesia in forefoot reconstruction surgery?

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN78024440

Enrollment

Registered

2006-09-29

Start date

2005-05-01

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

Surgery: Forefoot reconstruction Surgery Forefoot reconstruction

Interventions

Patients will be randomised into either the pain pump group or the standard technique group. All will receive a standardised general anaesthetic. Post operatively, visual analogue pain scores and pati

Eligibility

Inclusion criteria

Inclusion criteria: 30 patients undergoing forefoot reconstruction.

Exclusion criteria

Exclusion criteria: 1. Allergy to local anaesthetic 2. Any patient with previous surgery to that foot 3. Any patient requiring more extensive surgery e.g. Weil's osteonomies 4. Allergies/intolerances to NSAIDs

Design outcomes

Primary

Measure	Time frame
Visual Analogue pain scores. Patient satisfaction levels.	—

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