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A prospective, randomized controlled single center study exploring the impact of multimodal real-time identification and navigation tools on the efficiency of lumbar plexus block

A prospective, randomized controlled single center study exploring the impact of multimodal real-time identification and navigation tools on the efficiency of lumbar plexus block

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101058
Enrollment
Unknown
Registered
2025-04-18
Start date
2025-08-16
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Patients with advanced age or excessive obesity who undergo elective hip or knee replacement surgery for the first time

Interventions

Group A:Less-experienced middle-aged anesthesiologists complete ultrasound-guided lumbar plexus block with the assistance of multimodal real-time recognition and navigation tools
Group B :Experts use ultrasound alone to complete ultrasound-guided lumbar plexus block

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 110 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>75 years old or BMI > 35 Kg/m^2 6.ASA I-III levels 7.The patient has preoperative CT imaging results corresponding to the lumbar spine

Exclusion criteria

Exclusion criteria: 1.Abnormal coagulation function 2.Individuals with impaired mental health 3.Patients who are pregnant or breastfeeding 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 and depth of needle puncture;Minimal stimulation current;Analgesic dosage;Pain score;The time of the first request for emergency medication for pain relief;Complication;Satisfaction;

Countries

China

Contacts

Public ContactZhongyuan Xia

Renmin Hospital of Wuhan University

xiazhongyuan2005@aliyun.com+86 138 0862 8560

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026