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To Objective the security and effective of ultrasound combined nerve stimulator guided lumbar plexus nerve block in beach chair method

To Objective the security and effective of ultrasound combined nerve stimulator guided lumbar plexus nerve block in beach chair method

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-15007505
Enrollment
Unknown
Registered
2015-11-06
Start date
2015-10-11
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

arthroscopic surgery

Interventions

A:lumbar plexus nerve block in beach chair method
B:lumbar plexus nerve block in short axis plane method

Sponsors

The First Affiliated Hospital of Third Military Medical University, PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) aged 18-75 years old, men and women; (2) the proposed of unilateral the arthroscopic surgery patients; (3) the operating time is expected to less than 5 hours; (4) patients volunteered to participate in the research, and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) patients with emergency operation is proposed; (2) ASA levels - V or VI; (3) pregnant and breast-feeding women; (4) the recent aspirin or heparin drugs, anticoagulant therapy; (5) coagulant function is unusual; (6) allergy to local anesthetics; (7) bacteremia, sepsis patients or quasi puncture infection; (8) with nervous system disorders, spinal diseases, paresthesia, deformity of lower limb or outside of the injured; (9) hearing, vision, intelligence, mental anomaly and influence normal communicator; (10) patients with secondary surgery; (11) chronic pain therapy; (12) in recent 2 months to participate in other subjects; (13) the researchers think that should not be included in this test; Screening period shall not exceed two weeks with surgery.Involved in the research of the physician to can enter the screening of the subjects for the purpose of this clinical research situation were explained in detail and show "informed consent". Each subject at least 24 hours to fully considering whether to participate in this clinical trial. When the subjects or its agent, the guardian agreed and signed written informed consent, the record date accordingly.

Design outcomes

Primary

MeasureTime frame
Sensory block score of femoral nerve;Motor block score of the knee;Sensory block score of obturator nerve;Sensory block score of lateral femoral cutaneous nerve;Epidural spread;

Secondary

MeasureTime frame
Image positioning time;The depth of the puncture;times of the puncture;The puncture time;Intraoperative analgesia drug dosage;ptient’s satisfaction;complete recovery time of median nerve sensory block;complete recovery time of the keen joint activity;Postoperative VAS scores;The average blood pressure;The incidence of complications;

Countries

China

Contacts

Public ContactKaiZhi Lu

The First Affiliated Hospital of Third Military Medical University, PLA

lukaizhi@vip.tom.com+86 13608380096

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 7, 2026