Effect of ultrasound-guided erector spinae plane block on postoperative acute pain and the quality of recovery after breast cancer surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1800019599

Enrollment

Unknown

Registered

2018-11-19

Start date

2018-11-28

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

Breast Cancer

Interventions

experimental group:erector spinae plane block with 0.5% ropivacanine 25ml

control group:erector spinae plane block with 25 ml of normal saline

Eligibility

Sex/Gender

Female

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Eighty-two female participants (ASA status I or II, aged 18-65 years) scheduled for elective unilateral breast cancer surgery were assessed for study eligibility.

Exclusion criteria

Exclusion criteria: With history of allergy to local anesthetics, infection near the puncture site, chronic opioid use, inability to communicate, and other reasons that not appropriate for this study.

Design outcomes

Primary

Measure	Time frame
the quality of recovery;	—

Secondary

Measure	Time frame
Postoperative pain intensity at rest;Postoperative pain intensity at movement(deep breath);postoperative cumulative opioid consumption; the patient's satisfaction;Duration of PACU stay;	—

Countries

China

Contacts

Public ContactYusheng Yao

Fujian Provincial Hospital

fjslyys@126.com+86 13559939629

Outcome results

None listed

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