FindTrial
Sign In

The efficacy of continuous erector spinae plane block in post-operative of minimally invasive direct coronary artery bypass: a randomized controlled trial

The efficacy of continuous erector spinae plane block in post-operative of minimally invasive direct coronary artery bypass: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022388
Enrollment
Unknown
Registered
2019-04-09
Start date
2018-09-01
Completion date
Unknown
Last updated
2019-04-15

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

Conditions

Postoperative pain

Interventions

ESP Group:erector spinae plane block
ICNB Group:intercostal nerve block

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Aged 40-80 years, ASA II-III.

Exclusion criteria

Exclusion criteria: Contraindications of nerve block (abnormal coagulation function, puncture site infection, etc.); Inability to cooperate with the operation of nerve block (delirious or mentally abnormal patients); A history of spinal surgery or obvious thoracic spine abnormal; Ultrasound coupling agent, local anesthetic or opioid allergy; Long-term oral analgesics;Patients who refused to participate in this study.

Design outcomes

Primary

MeasureTime frame
Pain score;—

Secondary

MeasureTime frame
Analgesic rescue;—

Countries

China

Contacts

Public ContactLi Min

Peking University Third Hospital

liminanesth@aliyun.com+86 13522757239

Outcome results

None listed

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