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A prospective randomized controlled study of the perioperative analgesic effects of ultrasound-guided anterior sacral plexus + fascia iliaca compartment block one-point puncture versus fascia iliaca compartment block for intertrochanteric femoral fracture surgery

A prospective randomized controlled study of the perioperative analgesic effects of ultrasound-guided anterior sacral plexus + fascia iliaca compartment block one-point puncture versus fascia iliaca compartment block for intertrochanteric femoral fracture surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067638
Enrollment
Unknown
Registered
2023-01-16
Start date
2023-01-16
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

regional block

Interventions

anterior sacral plexus + fascia iliaca compartment block one-point puncture:ultrasound-guided anterior sacral plexus + fascia iliaca compartment block one-point puncture
fascia iliaca compartment block :ultrasound-guided fascia iliaca compartment block

Sponsors

Beijing Hospital of Traditional Chinese Medicine Huairou Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists (ASA) I-?, aged 18-85 years, BMI16-29kg/m2, who were scheduled for closed reduction and internal fixation of intertrochanteric fractures of the femur, were informed and consented to the study.

Exclusion criteria

Exclusion criteria: Patients with chronic pain; Puncture site infection; A history of allergy to any of the drugs used in the study; Obvious abnormal coagulation function; Severe liver, kidney or heart disease; Mental illness; Inability to understand and use PCIA; Refuse nerve blocks or use of postoperative analgesia pumps.

Design outcomes

Primary

MeasureTime frame
VAS score at 12 postoperative activities;

Secondary

MeasureTime frame
In the position of combine spinal-epidural blockd ?the VAS score at rest and activity 6h,24h and 48h after surgery and the VAS score at rest 12h after surgery;Total sufentanil consumption at 0-24 hours and 24-48 hours after surgery;The number of analgesic pump compressions within 48h after operation, the number of relief analgesia and the time of first analgesic pump compressions;The score was 24 hQOR-15 at 24h after surgery ;Time of first postoperative exhaust, time of getting out of bed and postoperative hospital stay;Incidence of postoperative adverse reactions;

Countries

China

Contacts

Public ContactYun Wang, Chunying Liao

Beijing Chaoyang Hospital,Capital Medical Unicersity/ Beijing Hospital of Traditional Chinese Medicine Huairou Hospital

wangyun129@ccmu.edu.cn+86 13521611825

Outcome results

None listed

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