Intraperitoneal bupivacaine for post-operative analgesia

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN86456561

Enrollment

Registered

2004-09-30

Start date

2003-11-04

Completion date

Unknown

Last updated

2022-11-21

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 Group 1: Bupivacaine + Saline (control) Group 2: Bupivacaine + Adept

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 35 patients in each group

Exclusion criteria

Exclusion criteria: Does not match inclusion criteria

Design outcomes

Primary

Measure	Time frame
Service outcome development	—

Secondary

Measure	Time frame
Not provided at time of registration	—

Countries

England, United Kingdom

Outcome results

None listed

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