Skip to content

Effects of Remote Ischemic Preconditioning With Postconditioning on Neurologic Outcome

Effects of Remote Ischemic Preconditioning With Postconditioning in Patients Undergoing Superficial Temporal Artery-middle Cerebral Artery (STA-MCA) Anastomosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03072914
Enrollment
108
Registered
2017-03-07
Start date
2017-03-07
Completion date
2018-07-15
Last updated
2018-08-23

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

Conditions

Moyamoya Disease, Remote Ischemic Preconditioning

Brief summary

In the present study, we evaluated whether RIPC with RIPostC reduce the major neurocomplication in patients undergoing STA-MCA anastomosis.

Interventions

PROCEDURERIPC with RIPostC

The sphygmomanometer is closed to the lower limb and the cuff is inflated and the pressure is increased by 30 mmHg higher than the systolic blood pressure of each patient for 5 minutes. The loss of the distal pulse is confirmed by Doppler in the dorsalis pedis pulse. If there is a pulse, increase the pressure until it disappears. After 5 minutes of ischemia time, the cuff is deflated to confirm that the pulse has returned and has a reperfusion time of 5 minutes. A total of 4 cycles of 5 cycles of ischemic time and 5 minutes of reperfusion time are performed. (Estimated total 40 minutes) When the skull is started to close, RIpc with RIPostC group performs RpostC and the method is the same as the above RIPC method. (Estimated total 40 minutes)

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. American Society of Anesthesiologists 2. Adults 18 to 65 years of age 3. In patients with planned MCA-STA anastomosis under general anesthesia 4. Patients who pre-agreed to the study

Exclusion criteria

1. If there is a history of peripheral vascular arterial or venous disease 2. If there is a previous history of peripheral nerve disease 3. Other brain or cerebrovascular disease 4. In case of serious cardiovascular disease, pulmonary disease, kidney disease 5. Patients who do not agree with the test

Design outcomes

Primary

MeasureTime frameDescription
Number of major adverse eventpostoperative one monthhyperperfusion syndrome, hypoperfusion, EDH, SAH, acute infarction

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026