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The effect of remote ischemic preconditioning on short-term perioperative neurocognitive disorders in patients with ischemic cerebrovascular disease undergoing spinal surgery: a randomized controlled trial

The effect of remote ischemic preconditioning on short-term perioperative neurocognitive disorders in patients with ischemic cerebrovascular disease undergoing spinal surgery: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099004
Enrollment
Unknown
Registered
2025-03-17
Start date
2025-03-17
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Ischemic cerebrovascular disease

Interventions

Sham group:Treatment was given 3 days before surgery, twice a day, 9-10 a.m., 4-5 p.m. Cuff pressure 60mmHg, pressurization 5min, open 5min, 5 cycles.
RIPreC group:Treatments were given 3 days before surgery, twice a day, 9-10 a.m., 4-5 p.m. Cuff pressure 200mmHg, pressurized 5min, open 5min, 5 cycles.

Sponsors

Xuanwu Hospital Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 45~80 years old; 2. ASA Class I.-III; 3. Elective interbody fusion; 4. Preoperative ischemic cerebrovascular disease, modified Rankin scale (MRS) score 0~3; 5. Able to understand and comply with the requirements of the clinical trial protocol, and voluntarily sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1. Patients who are intolerant to the pre-adaptation of distant ischemia; 2. Patients with unsatisfactorily controlled hypertensive diseases, i.e., resting systolic blood pressure >=180mmHg, and/or diastolic blood pressure >=110 mmHg; Patients with hypotension, i.e., resting systolic blood pressure < 90 mmHg, and/or diastolic blood pressure < 60 mmHg; 3. Other conditions judged by the investigator that the patient is not suitable to participate in the clinical study; 4. Emergency surgery; 5. Combined with severe organ insufficiency/failure; 6. Cognitive dysfunction before surgery; 7. Patients with severe language impairment, vision and hearing impairment who cannot complete the scale examination;

Design outcomes

Primary

MeasureTime frame
Incidence of short-term PND;Neurological complications;

Secondary

MeasureTime frame
Adverse event;Complications of other organ systems;Length of stay;Total cost of hospitalization;Inflammatory factors and markers related to neuroinflammation and nerve injury;RNA sequencing;

Countries

China

Contacts

Public ContactWang Tianlong

Xuanwu Hospital Capital Medical University

w_tl5595@hotmail.com+86 10 83199333

Outcome results

None listed

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