Ultrasound-guided modified thoracolumbar fascial plane block in Tianji robot assisted lumbar internal fixation: a prospective, randomized, and non-inferiority study.

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200058687

Enrollment

Unknown

Registered

2022-04-14

Start date

2022-04-01

Completion date

Unknown

Last updated

2024-01-14

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

Conditions

Pain after lumbar internal fixation assisted by skyline robot

Interventions

Ultrasound guided modified thoracolumbar fascia block group:Ultrasound guided modified thoracolumbar fascia block

Ultrasound guided thoracolumbar fascia block group:Ultrasound guided thoracolumbar fascia block

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologists (ASA) Class I to III; 2. Age range from 18 to 65; 3. Body mass index (BMI) 19-30 kg/m2; 4. Male and female patients who plan to receive Skyline robot-assisted lumbar internal fixation.

Exclusion criteria

Exclusion criteria: 1. Long-term use of opioids or steroids; 2. Coagulation disorders, therapeutic anticoagulation; 3. Pregnancy history.

Design outcomes

Primary

Measure	Time frame
Effective block area 30 minutes after block;	—

Secondary

Measure	Time frame
Nerve block operation time;Puncture times;Image clarity score;Patient satisfaction;Intraoperative sufentanil and remifentanil usage;Numeric Rating Scale, NRS;Amount of sufentanil used by PCIA;Amount of parecoxib recovery;Postoperative complications related to nerve block;Postoperative adverse reactions;Oswestry Disability Index;	—

Countries

China

Contacts

Public ContactHu Li

The Second Affiliated Hospital of Jiaxing University

517739395@qq.com+86 18257333506

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026