Investigation of Programmed Intermittent Bolus of Lumbar Plexus Block for Total Hip Arthroplasty

Investigation of Programmed Intermittent Bolus of Lumbar Plexus Block for Total Hip Arthroplasty - Investigation of PIB of LPB for THA

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000025774

Enrollment

Registered

2017-02-01

Start date

2017-02-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Total Hip Arthroplasty

Interventions

The set flow rate was continuous 6mL of levobupivacaine 0.1% every hour and 6mL levobupivacaine 0.1% lock out time: 60 minutes for 2 days. The set flow rate was intermittent bolus of 12mL of levobupiv

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who schedule THA

Exclusion criteria

Exclusion criteria: secondary surgery bilateral THA

Design outcomes

Primary

Measure	Time frame
Number of pushed PCEA The amount of fentanyl	—

Secondary

Measure	Time frame
Number of requested PCEA Number of patients used additional analgesi	—

Countries

Japan

Contacts

Public ContactHironobu Ueshima

Showa University Hospital Anesthesiology

ueshimhi@yahoo.co.jp0337848575

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026