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Effect of iliofascial block on the effective dose of lumbar anesthetic ropivacaine in the elderly

Effect of iliofascial block on the effective dose of lumbar anesthetic ropivacaine in the elderly

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103467
Enrollment
Unknown
Registered
2025-05-29
Start date
2023-02-24
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

hip fracture

Interventions

Iliac fascia block combined with lumbar anesthesia group:After 0.4% ropivacaine for iliofascial block, the effect of the block was assessed. If it was ineffective, the case was excluded, and those wh
lumbar anesthesia team:Lumbar anesthesia (L3-4 gap) was punctured and 0.5% ropivacaine was given. The initial dose of the drug was 6 mg of 0.5% ropivacaine, which was administered in a gradient of 0.5

Sponsors

Hainan General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 79 Years

Inclusion criteria

Inclusion criteria: (1) American Society of Anesthesiologists (ASA) class I-III; (2) Age 65-79 years old, weight 45-70 kg, height 150-180 cm, BMI: 18.5-23.9; (3) Hip replacement surgery in our hospital, and no contraindication to intralesional anesthesia; (4) No previous history of mental disorder and able to communicate or score normally; (5) No history of using sedative or analgesic drugs; (6) No infection in the FICB operation area; (7) Patients and their family members sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Psychiatric patients, patients unable to complete the scoring; (2) Patients with severe organ diseases such as congenital heart disease, cardiovascular disease and tumors; (3) Patients with hematopoietic dysfunction, immune system defects or organ function defects.

Design outcomes

Primary

MeasureTime frame
Half effective dose of ropivacaine required for lumbar anesthesia in both groups and its 95% confidence interval;

Secondary

MeasureTime frame
General patient information including age, gender, body mass index, and American Society of Anesthesiologists ASA classification were recorded;;Changes in vital signs (MAP, HR and SpO2) were recorded: the recording periods were before anesthesia (T0), 5 minutes after anesthesia (T1), 10 minutes after anesthesia (T2), 15 minutes after anesthesia (T3), at the time of skin incision (T4), 30 minutes after the beginning of the procedure (T5), and at the time of completion of the procedure (T6);;Patient Positioning Immediate Numeric Rating Scale Score;Motor Block Score; onset of anesthesia;Time for anesthesia to wear off;Duration of analgesia;

Countries

China

Contacts

Public ContactLin Hui

Hainan General Hospital

linhui7811@126.com+86 133 2200 4163

Outcome results

None listed

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