Study for postoperative pain control of continuous trans-catheter local anesthetic

Study for postoperative pain control of continuous trans-catheter local anesthetic - Study for postoperative pain control of continuous trans-catheter local anesthetic

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000025488

Enrollment

100

Registered

2017-01-02

Start date

2017-01-10

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

cardiac valve diseade

Interventions

0.25% levobupivacaine at 4 ml / h using a porous catheter, continuous administration until the first day after surgery on the wound site

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patient scheduled to undergo catheterization using a transapical apical approach with agreement before surgery

Exclusion criteria

Exclusion criteria: Local anesthetic drug allergy

Design outcomes

Primary

Measure	Time frame
assessment of postoperative analgesia score (NRS)	—

Secondary

Measure	Time frame
postoperative blood pressure, heart rate, SpO 2, time to leave, length of stay in hospital, presence of cardiovascular complications, respiratory complications With or without	—

Countries

Japan

Contacts

Public ContactYumi Obata

St. marianna University school of Medicine Anesthesiology

y2obata@marianna-u.ac.jp044-977-8111

Outcome results

None listed

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