The study of clinical usefulness of Erector Spinae Plane block in spinal surgery

The study of clinical usefulness of Erector Spinae Plane block in spinal surgery - The study of clinical usefulness of Erector Spinae Plane block in spinal surgery

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000037136

Enrollment

110

Registered

2019-06-25

Start date

2019-03-01

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

Lumbar spine disease

Interventions

In the block group, the spinae erector plane block is administered after induction of anesthesia. (Use 40 ml of 0.375% ropivacaine) The control group performs anesthesia management as usual.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Patients who undergo lumbar spine surgery 2) ASA-PS 1 or 2 3) Patients with surgery time within 3 hours and surgery site up to 3 4) Regarding the participation in this research, the person has obtained written consent by free will

Exclusion criteria

Exclusion criteria: 1) After lumbar spine posterior fixation surgery 2) Emergency operation patients 3) Patients who can not obtain research consent 4) Preoperative NRS is 7 or more 5) Patients judged to be inappropriate by the investigator or in charge of the research

Design outcomes

Primary

Measure	Time frame
Preoperative and postoperative pain scale(NRS)	—

Secondary

Measure	Time frame
Intraoperative drug use, Postoperative analgesic use	—

Countries

Japan

Contacts

Public ContactShuji Kurokawa

Konan Kosei Hospital Anesthesiology

kurokawa@aichi-med-u.ac.jp0587513333

Outcome results

None listed

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