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Comparison of the Effects of Erector Spinae Plane Block versus Fascia Iliaca Compartment Block on Postoperative Recovery Quality after Posterior Total Hip Arthroplasty: A Single-Center, Double-Blind, Randomized Controlled Trial

Comparison of the Effects of Erector Spinae Plane Block versus Fascia Iliaca Compartment Block on Postoperative Recovery Quality after Posterior Total Hip Arthroplasty: A Single-Center, Double-Blind, Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119889
Enrollment
Unknown
Registered
2026-03-05
Start date
2026-03-10
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Severe postoperative pain after posterior total hip arthroplasty (THA)

Interventions

Erector Spinae Plane Block Group:Erector Spinae Plane Block at the L4 Level
Fascia Iliaca Compartment Block Group:Suprainguinal Fascia Iliaca Compartment Block

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Age: 45-85 years old; 2.ASA:I-III; 3.Undergoing unilateral total hip replacement (THR) via the posterolateral approach for the following indications: hip osteoarthritis, avascular necrosis of the femoral head, developmental dysplasia of the hip; 4.Providing informed consent.

Exclusion criteria

Exclusion criteria: 1.Long-term use of opioids, a history of preoperative analgesic abuse (> 3 months), or a history of chronic pain other than joint diseases; 2.Presence of contraindications to regional anesthesia (such as coagulation disorders, infection at the puncture site, local anesthetic allergy, etc.); 3.Emergency surgery or revision surgery; 4.Total hip replacement (THR) performed under neuraxial anesthesia; 5.History of local spinal lesions or spinal surgery; 6.Pregnancy/lactation period; 7.Comorbidity of severe cardiac insufficiency (New York Heart Association [NYHA] classification >= Class III), hepatic insufficiency (Child-Pugh classification >= Class C), or renal impairment (serum creatinine > 442 µmol/L or glomerular filtration rate [GFR] < 60 mL/min); 8.Previous history of neurological or psychiatric disorders; 9.Planned postoperative admission to the intensive care unit (ICU); 10.Presence of cognitive impairment, language communication disorders, inability to cooperate with the study procedures, or refusal to participate.

Design outcomes

Primary

MeasureTime frame
Quality of Recovery - 15;

Secondary

MeasureTime frame
The time of the first getting out of bed after surgery.;Manual Muscle Test (MMT) score of the quadriceps;The first pressing time of the postoperative analgesic pump;The time of the first rescue analgesia, the incidence rate of rescue analgesia, and the dosage of drugs used for rescue analgesia.;The occurrence situations of postoperative infection, hematoma, subcutaneous emphysema, shoulder pain, local anesthetic poisoning, etc.;Modified Bromage Score;Postoperative opioid consumption (in morphine equivalents) at 6 hours, 12 hours, 24 hours, and 48 hours;Numerical Rating Scale;

Countries

China

Contacts

Public ContactMengxing Jia

The Affiliated Hospital of Xuzhou Medical University

jmx5278@163.com+86 516 85802297

Outcome results

None listed

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