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Comparison of the Efficacy and Safety of Lumbosacral Plexus Combined with Lateral Femoral Cutaneous Nerve Block versus Fascia Iliaca Block for Postoperative Analgesia in Hip Arthroplasty: A Single-Center, Randomized, Controlled Trial

Comparison of the Efficacy and Safety of Lumbosacral Plexus Combined with Lateral Femoral Cutaneous Nerve Block versus Fascia Iliaca Block for Postoperative Analgesia in Hip Arthroplasty: A Single-Center, Randomized, Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119354
Enrollment
Unknown
Registered
2026-02-26
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

None

Interventions

Group B:Lumbosacral plexus combined with lateral femoral cutaneous nerve block using 0.15% ropivacaine with 4 µg/kg hydromorphone (total volume 40 mL)
Group C:Fascia iliaca compartment nerve block performed with 0.2% ropivacaine combined with hydromorphone 4 µg/kg (total volume 40 mL)
Group A:Lumbosacral plexus combined with lateral femoral cutaneous nerve block using 0.2% ropivacaine with 4 µg/kg hydromorphone (total volume 40 mL)

Sponsors

Hainan General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients scheduled to undergo hip arthroplasty; 2.Age: >=18 years; 3.Body mass index (BMI): 18–28 kg/m^2; 4. American Society of Anesthesiologists (ASA) physical status classification ?–? 5. Ability to communicate normally; 6.Complete clinical data 7.Voluntary participation and signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Presence of contraindications to combined spinal-epidural anesthesia or fascia iliaca compartment block 2.Allergy to ropivacaine or hydromorphone 3.Preoperative cognitive impairmen 4.Severe hepatic or renal dysfunction 5.Long-term use of opioid analgesics 6.Participation in any drug clinical trial within 1 month prior to screening 7.Any other condition deemed by the investigator as inappropriate for participation in this trial 8.Refusal to participate in this study.

Design outcomes

Primary

MeasureTime frame
Postoperative pain intensity;The incidence of rescue analgesia within 72 hours postoperatively and the time to first rescue analgesic requirement.;

Secondary

MeasureTime frame
Incidence of adverse reactions;Postoperative rehabilitation-related parameters;Analgesia-related parameters;

Countries

China

Contacts

Public ContactGao Wei

Hainan General Hospital

gaowei20055@126.com+86 898 6864 2232

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026