Skip to content

Effect of Ulinastatin Combined with Ginkgo Biloba Extract on Postoperative Delirium in Elderly Patients Undergoing Hip Surgery: A Randomized Controlled Trial

Effect of Ulinastatin Combined with Ginkgo Biloba Extract on Postoperative Delirium in Elderly Patients Undergoing Hip Surgery: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128312
Enrollment
Unknown
Registered
2026-07-17
Start date
2024-09-19
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Postoperative delirium

Interventions

Ulinastatin combined with Ginkgo biloba extract group (UE group):Ulinastatin 5000 u/kg intravenously infused via pump over 15 min, and Ginkgo biloba extract injection 70 mg per dose added to 250 mL no
Control group (C group):Equal volume of normal saline intravenously administered at the same time points before incision and days 1-3 after surgery

Sponsors

Tianjin Jizhou District People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
70 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=70 years; 2. American Society of Anesthesiologists (ASA) physical status classification I-III; 3. Scheduled to undergo hip surgery under ultrasound-guided fascia iliaca compartment block combined with combined spinal-epidural anesthesia; 4. Preoperative hepatic and renal functions, acid-base balance, blood glucose, and serum electrolytes are within normal limits.

Exclusion criteria

Exclusion criteria: 1. Patients with current or previous central nervous system diseases; 2. Patients with active liver disease, or those who have previously undergone neurosurgery or cardiac surgery; 3. Patients who have used sedatives or antidepressants during the study period; 4. Patients with severe visual or auditory impairment, or those who are unable to understand Mandarin; 5. Patients who have previously been exposed to the same neuropsychological scales; 6. Patients with a preoperative Mini-Mental State Examination (MMSE) score of less than or equal to 24; 7. Patients with poor compliance or those who are unable to complete the trial in accordance with the study protocol; 8. Patients who have participated in other clinical drug trials within the past 4 weeks; 9. Patients who are deemed unsuitable for inclusion by the investigator for any reason.

Design outcomes

Secondary

MeasureTime frame
Postoperative delirium incidence rate;Duration of postoperative delirium;Serum interleukin-6 (IL-6) level;Serum S100 calcium-binding protein B (S100ß) level;Postoperative delirium incidence rate and associated complications;

Countries

China

Contacts

Public ContactWang Ruyi

Tianjin Jizhou District People’s Hospital

ruyiwang36@163.com+86 131 1607 6303

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026