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A prospective, randomized controlled single center study exploring the effect of artificial intelligence assisted recognition system on the efficiency of lumbar plexus block

A prospective, randomized controlled single center study exploring the effect of artificial intelligence assisted recognition system on the efficiency of lumbar plexus block

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100685
Enrollment
Unknown
Registered
2025-04-14
Start date
2025-04-30
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Perioperative analgesia for patients undergoing their first elective hip or knee replacement surgery

Interventions

Group A:Experienced middle-aged anesthesiologists complete ultrasound-guided lumbar plexus block with the assistance of an artificial intelligence assisted recognition system
Group B:Expert anesthesiologists complete ultrasound-guided lumbar plexus block

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Voluntary signing of informed consent form; 2.Promise to comply with research procedures and cooperate in implementing the entire research process; 3.Selective first hip or knee replacement surgery; 4.Gender is not limited; 5.Age between 18-75 years old (inclusive) and 18 <= BMI <= 35 kg/m^2; 6.ASA I-III levels

Exclusion criteria

Exclusion criteria: 1.Abnormal coagulation function; 2.Insufficiency of mind; 3.Pregnant or breastfeeding individuals; 4.Diabetes peripheral neuropathy; 5.Participated in other clinical trials within the past three months; 6.Refusal to participate; 7.Equipped with specific devices (such as pacemakers); 8.History of stroke; 9.Infection at the puncture site; 10.Allergies to local anesthetics or coupling agents; 11.Patients receiving chronic analgesic treatment with opioid drugs

Design outcomes

Primary

MeasureTime frame
Success rate of block;

Secondary

MeasureTime frame
Time consumption of block;The puncture frequency of needle puncture;Failure Rate;Minimal stimulation current;Intraoperative analgesic dosage;Changes in vital signs;Surgical duration;Adverse events;

Countries

China

Contacts

Public ContactZhongyuan Xia

Renmin Hospital of Wuhan University

984188203@qq.com+86 138 0862 8560

Outcome results

None listed

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