A randomised double-blind trial to investigate the efficacy of intra-articular bupivacaine for pain relief following ankle arthroscopy

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN07238689

Enrollment

Registered

2003-09-12

Start date

2003-03-01

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

1. Normal saline 2. 0.5% Bupivacaine

Eligibility

Inclusion criteria

Inclusion criteria: 48 patients aged =18 years old undergoing day case ankle arthroscopy who have given informed written consent.

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

Measure	Time frame
Not provided at time of registration	—

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