A prospective randomised double-blinded comparison of 0.125% and 0.0625% bupivicaine for the management of postoperative pain in patients undergoing major abdominal surgery.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN45045119

Enrollment

Registered

2003-09-12

Start date

2002-05-31

Completion date

Unknown

Last updated

2020-03-03

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

Conditions

Signs and Symptoms: Post operative pain Surgery

Interventions

Randomised controlled trial and telephone interviews for patient centered phase

Eligibility

Inclusion criteria

Inclusion criteria: 86 patients undergoing major abdominal surgery nursed with epidural for postoperative pain relief, randomised to two groups

Exclusion criteria

Exclusion criteria: Does not meet inclusion criteria

Design outcomes

Primary

Measure	Time frame
Pain relief response to therapy	—

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