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Application of ultrasound-guided lumbar plexus block and erector spinal nerve block in femoral head replacement: a multicenter, randomized controlled study.

Application of ultrasound-guided lumbar plexus block and erector spinal nerve block in femoral head replacement: a multicenter, randomized controlled study.

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043809
Enrollment
Unknown
Registered
2021-03-04
Start date
2021-03-05
Completion date
Unknown
Last updated
2021-06-28

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

Conditions

Femoral head replacement

Interventions

Erector spinal nerve block group:Erector spinal nerve block
Lumbar plexus block group:Lumbar plexus block
Control group:Nil

Sponsors

Affiliated Hospital of Jiaxing College, Jiaxing City, Zhejiang Province
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Source and expected number of cases: from March 2021 to May 2021, one hundred and twenty patients, aged 18-80 years, ASA I- III, BMI18.5~23.9kg/m2, underwent elective unilateral femoral head replacement and general anesthesia in the first and second Hospital of Jiaxing City.

Exclusion criteria

Exclusion criteria: (1) Shock or coma; (2) abnormal function of heart, lung, liver, kidney and blood coagulation; (3) infection in the planned block area and severe nerve injury in the limb; (4) history of chronic pain, history of taking analgesics, history of taking psychiatric diseases, history of radiotherapy and chemotherapy, patients with contraindications to non-steroidal anti-inflammatory drugs; (5) patients who are allergic to local anesthetic drugs such as lidocaine, ropivacaine and general anesthetics. (6) patients and their families refused surgical anesthesia.

Design outcomes

Primary

MeasureTime frame
All aspects of recovery quality score (QoR-40) before and 24 hours after operation.;

Secondary

MeasureTime frame
NRS scores of rest and exercise at 0.5 h, 1 h, 3 h, 6 h, 12 h, 18 h and 24 h after operation;First analgesia relief time;Times of pump pressing for postoperative analgesia;Total dosage of Shufen 24 hours after operation;All postoperative adverse reactions such as hypotension, respiratory depression, tremor and urinary retention;

Countries

China

Contacts

Public ContactWei Deng

Affiliated Hospital of Jiaxing College

dengwei1992868@163.com+86 19884340796

Outcome results

None listed

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