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The clinical study on ultrasound-guided retrolaminal block for patients undergoing scoliosis surgery

The clinical study on ultrasound-guided retrolaminal block for patients undergoing scoliosis surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026248
Enrollment
Unknown
Registered
2019-09-28
Start date
2019-10-14
Completion date
Unknown
Last updated
2019-09-30

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

Conditions

Pain

Interventions

Experimental group:Combined ultrasound-guided retrolaminal block and general anesthesia
Control group:General anesthesia

Sponsors

The First Affiliated Hospital of GuangXi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. aged 18 to 65 years; 2. scheduled to undergo scoliosis surgery; 3. American Society of Anesthesiologists (ASA) physical status classification of I - III.

Exclusion criteria

Exclusion criteria: 1. body mass index (BMI) > 32 kg/m2; 2. contraindications for regional anesthesia; 3. opioid dependence; 4. peripheral neuropathy; 5. hepatic or renal insufficiency; 6. coagulopathy; 7. cardiopulmonary dysfunction; 8. allergy to local anesthetics or other medications.

Design outcomes

Primary

MeasureTime frame
VAS scores;The dosage of propofol;The dosage of fentanyl;The dosage of remifentanyl;Time of extracted the endotracheal tube;—

Countries

China

Contacts

Public ContactWenzheng He

The First Affiliated Hospital of Guangxi Medical University

he20082008@126.com+86 13481122163

Outcome results

None listed

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