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Effect of lumbar plexus block combined with dexmedetomidine on postoperative delirium in elderly patients with hip fractures: A prospective, randomized controlled trial

Effect of continuous lumbar plexus block combined with dexmedetomidine on postoperative delirium in elderly patients with hip fractures: a prospective, randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021549
Enrollment
Unknown
Registered
2019-02-27
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-03-04

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

Conditions

Hip Fractures

Interventions

DG:Dexmedetomidine was intravenously administered 0.1 g/kg/h the day before surgery
RG:On the day before the operation, the posterior lumbar plexus block (0.375% ropivacaine, 30ml) was performed by an experienced anesthesiologist under ultrasound guidance and catheterization was perf
RDG:continuous intravenous dexmedetomidine (0.1 g/kg/h) at the same time of continuous lumbar plexus block one day before the surgery, which was maintained during the surgery until 48h after the surge

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Elderly patients with hip fracture who receive elective surgical treatment; 2) Aged 65 years and above; 3) ASA I ~ III; 4) Sign informed consent.

Exclusion criteria

Exclusion criteria: 1) Cmpound injury: multiple fractures, combined with trauma of the head, chest, abdomen, pelvis and other parts other than the hip 2) Contraindications for lumbar plexus block: puncture site infection, peripheral neuropathy, local anesthetic allergy, etc 3) Co-existing neurological diseases: alzheimer's disease, vascular dementia and other diseases that affect the cognitive function of patients 4) There is an allergy to the test drug 5) Have participated in other clinical trials

Design outcomes

Primary

MeasureTime frame
POD;

Secondary

MeasureTime frame
type and severity of POD;postoperative pain;postoperative inflammatory biomarkers;postoperative complications;drug use;mortality;quality of life;

Countries

China

Contacts

Public ContactJinBao LI

Shanghai General Hospital

lijinbaoshanghai@163.com+86 15021928910

Outcome results

None listed

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