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Does continuous epidural infusion as post-operative analgesia alter outcomes in patients undergoing joint arthroplasty?

Does continuous epidural infusion as post-operative analgesia alter outcomes in patients undergoing joint arthroplasty?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN16744195
Enrollment
Unknown
Registered
2003-09-12
Start date
2002-11-01
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

Group 1 - epidural Group 2 - patient-controlled analgesia

Sponsors

Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult elective primary artheroplasty patients

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Pain score, side effects, patient satisfaction, demographics, time to discharge, blood loss, deviance from the integrated care pathway, loss of movement, time to mobilisation.—

Secondary

MeasureTime frame
Not provided at time of registration—

Countries

United Kingdom

Outcome results

None listed

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