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Effect of continuous erector spinae plane block on postoperative recovery in patients undergoing minimally invasive cardiac surgery

Effect of continuous erector spinae plane block on postoperative recovery in patients undergoing minimally invasive cardiac surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090487
Enrollment
Unknown
Registered
2024-09-30
Start date
2022-01-18
Completion date
Unknown
Last updated
2024-10-07

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

Conditions

Patients undergoing minimally invasive cardiac surgery

Interventions

Controll Group:continuous erector spinal plane block with 0.9% NaCl
ESPB Group:continuous erector spinal plane block with 0.375%/0.2% ropivacaine

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing minimally cardiac surgery with elective cardiopulmonary bypass via intercostal incision; 2. No gender limitation, age between 18 and 80 years old; 3. ASA classification I-III; 4. EuroScore <5; 5. Body mass index (BMI) <31 kg/m^2; 6. Understand and administer the Postoperative Intravenous Analgesia Pump (PCIA) independently or with assistance.

Exclusion criteria

Exclusion criteria: 1. Refuse to participate or unable to communicate; 2. Participating in other clinical trials; 3. Contraindications of nerve block, including infection at puncture site, severe coagulopathy and severe spinal deformity; 4. Patients with neurocognitive impairment (NCD), depression and other mental diseases before surgery, or unable to complete the postoperative scale; 5. Long-term use of analgesics, or known abuse of alcohol, drugs or narcotic drugs; 6. Accompanied by other conditions, such as breastfeeding, pregnancy, tumor, severe disability, etc.

Design outcomes

Primary

MeasureTime frame
QoR-15 score 24h after surgery;

Secondary

MeasureTime frame
QoR-15 score 48h after surgery;QoR-15 score 72h after surgery;VAS score;Amount of sufentanil;Remedial analgesia rate;Nausea and vomiting;Mechanical ventilation duration;Duration of ICU stay;The hospitalization time;chronic pain;

Countries

China

Contacts

Public ContactGUO KEFANG

Zhongshan Hospital, Fudan University

guo.kefang@zs-hospital.sh.cn+86 138 1770 6936

Outcome results

None listed

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