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Effects of continuous fascia iliaca compartment block guided by ultrasound on postoperative pain and early recovery in patients undergoing total knee arthroplasty

Effects of continuous fascia iliaca compartment block guided by ultrasound on postoperative pain and functional recovery in preoperative pain sensitive total knee arthroplasty patients

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045867
Enrollment
Unknown
Registered
2021-04-25
Start date
2021-05-01
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

orthopedic surgery

Interventions

Group F:continuous fascial iliac compartment block and Local infiltration anesthesia
Group L:Local infiltration anesthesia

Sponsors

The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with osteoarthritis who underwent unilateral total knee arthroplasty for the first time in the orthopedics department of our hospital from May 2021 to October 2021. 2. ASA I-III level, aged 50-75 years, no gender limits. 3. BMI 18-30Kg/m^2. 4. No history of mental illness, hearing impairment, or language impairment.

Exclusion criteria

Exclusion criteria: 1. With a history of anaesthetic allergy, infection at the puncture site, coagulation dysfunction, and peripheral nervous system disorders. 2. The patient or family members refused to perform nerve block. 3. Long-term use of analgesic, sedative drugs or alcohol or drug abuse. 4. Patients with severe liver and kidney dysfunction. 5. Patients with severe cardiovascular disease. 6. Patients with severe lung damage.

Design outcomes

Primary

MeasureTime frame
numeric rating scale;pressure pain threshold;the proportion of patient with moderate/severe pain during a 5 meter walk test 24 hours postoperatively;

Secondary

MeasureTime frame
postoperative exhaust time;number of postoperative analgesic remedies;the proportion of patient with moderate/severe pain during a 5 meter walk test 48 hours postoperatively;first time to get out of bed;postoperative hospital stay;

Countries

China

Contacts

Public ContactWang Di

The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China

13515604253@163.com+86 13515604253

Outcome results

None listed

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