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Effect of Sedation Depth on Postoperative Delirium in Elderly Patients Undergoing Hip Fracture Surgery with Nerve Block

Effect of Sedation Depth on Postoperative Delirium in Elderly Patients Undergoing Hip Fracture Surgery with Nerve Block

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031997
Enrollment
Unknown
Registered
2020-04-17
Start date
2020-04-27
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

Postoperative Delirium

Interventions

Deep sedation group:BIS:50~70
Light sedation group :BIS:71~90

Sponsors

Central Hospital of Zibo City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
80 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade I~III; 2. Aged no less than 80 years; 3. no existed delirium determined by CAM method; 4. MMSE score >= 15.

Exclusion criteria

Exclusion criteria: (1) previous psychiatric (depression, schizophrenia) or neurological (stroke, transient ischemic attack, epilepsy, brain trauma, etc.) history; (2) severe visual and hearing impairment; (3) long-term use of sedative-hypnotic drugs and antipsychotic drugs; (4) excessive drinking;Alcohol dependence self rating > 2; (5) patients with pulmonary infection and COPD; (6) severe liver and kidney dysfunction (AST or ALT 1.5 times over normal, Cr or BUN over normal); (7) myocardial infarction or congestive heart failure within 6 months (NYHA grade IV); (8) allergic to local anesthetic drugs or propofol; (9) contraindications of nerve blocks such as puncture site infection, coagulation dysfunction, and peripheral neuropathy; (10) other fractures, bilateral hip fractures or previous history of hip fractures; (11) if the nerve block fails or the effect is poor, the patient changes to general anesthesia with auxiliary laryngeal mask or endotracheal intubation; (12) the operative time was more than 2.5 hours, or the intraoperative hemorrhage was more than 600ml.

Design outcomes

Primary

MeasureTime frame
POD;

Secondary

MeasureTime frame
ADLs;VAS;BIS;

Countries

China

Contacts

Public ContactJiguo Si

Central Hospital of Zibo

43254465@qq.com+86 18678186929

Outcome results

None listed

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