Skip to content

Effect of tranexamic acid on cognitive function of elderly patients after non-cardiac surgery

Effect of tranexamic acid on cognitive function of elderly patients after non-cardiac surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056462
Enrollment
Unknown
Registered
2022-02-06
Start date
2021-12-02
Completion date
Unknown
Last updated
2024-10-15

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

Conditions

postoperative neurocognitive disorders

Interventions

Group A:single bolus of 20 mg/kg IV-TXA diluted 100ml before skin incision
Group B:normal saline in total 100 ml volume intravenous administration before operation.

Sponsors

The Fourth Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 65 to 80 years old, no gender limit; 2. Patients who plan to undergo non-cardiac and non-neurosurgical surgery under general anesthesia; 3. No tranexamic acid taboo; 4. All patients were screened with a Informant Questionnaire on Cognitive Decline (IQCODE) > 51, Montreal cognitive assessment (MoCA) (MoCA <= 13(illiterate), MoCA <= 19(primary school), MoCA <= 2(Middle school or above)), Clinical Dementia Rating (CDR) of 0.5 points, and fully capable of basic activities of daily living those were identified with mild cognitive impairment (MCI) before the surgery; 5. All patients have the ability to act in full spirit, understand and sign the informed consent, and are willing to complete the whole research process.

Exclusion criteria

Exclusion criteria: 1. Planned use of systemic TXA during surgery; 2. Preoperative hepatic or renal dysfunction; 3. Preoperative use of anticoagular medication seven days prior to surgery; 4. History of fibrinolytic disorder or blood dyscrasia; 5. Cerebrovascular accident, myocardial infarction, New York heart association class III or IV heart failure, atrial fibrillation, history of deep vein thrombosis or pulmonary embolus; 6. History of seizure disorder; 7. In the last 3 months, they have participated in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Postoperative delirium;

Secondary

MeasureTime frame
Postoperative cognitive dysfunction;Systemic inflammation level;Intraoperative blood loss;

Countries

China

Contacts

Public ContactQi Sihua

The Fourth Affiliated Hospital of Harbin Medical University

xyy85805066@126.com+86 15245066070

Outcome results

None listed

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