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effects of paravertebral block on postoperative analgesia in children undergoing lateral incision cardiac surgery with cardiopulmonary bypass: a randomized controlled trial

effects of paravertebral block on postoperative analgesia in children undergoing lateral incision cardiac surgery with cardiopulmonary bypass: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081773
Enrollment
Unknown
Registered
2024-03-11
Start date
2024-03-11
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

postoperative pain of pediatric cardiac surgery

Interventions

paravertebral block group (experimental group):After surgery, patients in the experimental group undergo paravertebral block using drug A, and local infiltration anesthesia using drug B. For the exper
local infiltration anesthesia group (control group):After surgery, patients in the control group undergo paravertebral block using drug A, and local infiltration anesthesia using drug B. For the exper

Sponsors

Fuwai Hospital, National Center for Cardiovascular Diseases
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 14 Years

Inclusion criteria

Inclusion criteria: (1) Children aged 6-14 years old; (2) Children who have atrial septal defect or ventricular septal defect scheduled for lateral incision cardiac surgery with cardiopulmonary bypass; (3) Inform consent signed by the parent or legal guardian.

Exclusion criteria

Exclusion criteria: (1) Patients who were intubated, on mechanical circulatory support, or with intravenous inotropes before surgery; (2) Emergency surgery or redo cardiac surgery; (3) Body weight more than 50 kg; (4) Diagnosed as severe pulmonary hypertension; (5) Left ventricular ejection fraction less than 45% in most recent echocardiography before surgery; (6) Allergic to ropivacaine or other regular anesthetics, analgesics or other medications regularly used in the study; (7) Preoperative platelet counts less than 100*109/L, coagulopathy or bleeding tendency ; (8) Preoperatively using antiplatelets or anticoagulants; (9) Diagnosed with scoliosis or other contraindications for PVB.

Design outcomes

Primary

MeasureTime frame
total opioid consumption during the first 24h after surgery;

Secondary

MeasureTime frame
FPS-R score at 6h, 12h, 18h, 24h postoperatively;The rate of opioid treatment for remedial analgesia between groups;The first time of FPS-R=4 postoperatively;

Countries

China

Contacts

Public ContactJingfei Guo

Fuwai Hospital, National Center for Cardiovascular Diseases

trhsbcq@163.com+86 158 1039 6387

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026