Skip to content

Effect of ultrasound - guided erector spinae plane block VS thoracic paravertebral nerve block on acute and chronic pain after Radical mastectomy: a randomized, controlled clinical study

Effect of ultrasound - guided erector spinae plane block VS thoracic paravertebral nerve block on acute and chronic pain after Radical mastectomy: a randomized, controlled clinical study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015217
Enrollment
Unknown
Registered
2018-03-15
Start date
2018-03-11
Completion date
Unknown
Last updated
2018-05-28

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

Conditions

Acute and chronic pain after Radical mastectomy

Interventions

Ultrasound guided thoracic paravertebral nerve block group(T):Before the induction of anesthesia, 20ml of 0.375% ropivacaine was injected into the thoracic paravertebral space between T4 and T5 on t
ultrasound guided erector spinae plane block group (E):Before the induction of anesthesia, 20ml of 0.375% ropivacaine was injected into the erector spinae plane at T4 level on the surgical side under
Control group (C):Before the induction of anesthesia 20ml of saline was injected into the Subcutaneous tissue at T4 level on the surgical side under ultrasound guidance

Sponsors

The Second Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: A total of 90 patients undergoing Radical mastectomy under general anesthesia were selected; ASA I-II; aged 20-80 years; ethical, voluntary and signed informed consent.

Exclusion criteria

Exclusion criteria: Severe spine deformity; puncture site infection; anticoagulant therapy; morbid obesity (BMI> 40kg/m2); local anesthetic drug allergy; severe heart and lung disease; liver and kidney dysfunction; patients with mental illness, speech and communication disorders

Design outcomes

Primary

MeasureTime frame
Cumulative dose of opioids in 24h?48h after surgery;2h, 4h, 8h, 24h, 48h after operation, VAS scores for rest and exercise, and rest and exercise VAS scores for 3 months after operation;Postoperative nausea and vomiting, dizziness, respiratory depression, adverse reactions to urinary retention;

Secondary

MeasureTime frame
The first time and the number of compressions of analgesic pump within 48 hours;postoperative analgesia satisfaction score;Changes in blood pressure and heart rate before and after skin incision;Wake-up time and extubation tim;Days of Postoperative hospital stay;

Countries

China

Contacts

Public ContactZhenzhong Luo

The Second Affiliated Hospital of Nanchang University

luozhenzhong@163.com+86 13970072357

Outcome results

None listed

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