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Circum-psoas block versus supra-inguinal fascia iliaca block in hip arthroplasty: a randomized controlled study

Circum-psoas block versus supra-inguinal fascia iliaca block in hip arthroplasty: a randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053421
Enrollment
Unknown
Registered
2021-11-20
Start date
2021-12-31
Completion date
Unknown
Last updated
2022-09-26

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

Conditions

None listed

Interventions

crico-psoas block group:ultrasound-guided circum-psoas block
Inguinal ligament suprafascia iliaca block group:supra-inguinal fascia iliaca block

Sponsors

Beijing Chaoyang Hospital, Capital Medical Univeristy
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. SA I-III level; Aged 18-90 years; 2. BMI 18-30kg/m^2; 3. Elective hip replacement surgery; 4. Liver and kidney function are normal; 5. Patients were aware of this study and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Puncture point infection; 2. Anticoagulation state; 3. Allergy to local anesthetics; 4. Serious cardiovascular disease, blood disease; 5. Long-term use of opioids or alcohol abuse; 6. Combined with myasthenia gravis or Parkinson's disease or pregnancy status; 7. History of previous hip or spine surgery; 8. Cognitive dysfunction before surgery, unable to cooperate with pain assessment; 9. Narrowing of the space between the sacral wing and the transverse process of L5.

Design outcomes

Primary

MeasureTime frame
dynamic pain scores;

Secondary

MeasureTime frame
static pain scores;dynamic pain scores at 12, 24 and 48 hours after surgery;sensory block;motor block;first opioid request;duration of surgery;length of hospital stay;patient satisfaction;adverse events (vascular puncture, nerve injury, local anesthetic toxicity, dizziness, nausea, vomiting, urinary retention, respiratory depression);opioid consumption at 24 h and 48 h after surgery;

Countries

China

Contacts

Public ContactWang Yun

Beijing Chaoyang Hospital, Capital Medical Universit

wangyun129@ccmu.edu.cn+86 13521611825

Outcome results

None listed

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