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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03089814
Other study ID # RIPC-VOT
Secondary ID
Status Completed
Phase N/A
First received March 14, 2017
Last updated February 26, 2018
Start date March 23, 2017
Est. completion date July 10, 2017

Study information

Verified date February 2018
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Changes in tissue microcirculation during ischemic conditioning (4 cycles of 5-min ischemia and 5-min reperfusion) has not been well documented. In previous studies, there was difference in changes in microcirculation, such as recovery slope and occlusion slope, between healthy subjects and cardiac surgery patients. Moreover, the occlusion slope, which reflects local tissue oxygen consumption during ischemic period, is anticipated to decrease during repeated ischemia-reperfusion cycle by its protecting effect, however there has not been well-conducted study. The purpose of the study is to evaluate the changes in microcirculation measured by tissue oxygen saturation during ischemic conditioning between healthy volunteers and cardiac surgery patients.


Description:

Subjects who are male healthy volunteers (aged 20-45) or who are scheduled to receive cardiac surgery (aged 20-80) will undergo ischemic conditioning, consisting of 4 cycles of 5-min ischemia with pressure of 200 mmHg on upper extremity followed by 5-min reperfusion with no pressure. During ischemic conditioning, changes in tissue microcirculation (baseline tissue saturation, occlusion slope during ischemia, and recovery slope during reperfusion) will be observed using tissue oxygen saturation sensor attached to the thenar muscle of the hand. For cardiac surgery patients, the study will be conducted before anesthesia induction on the surgery day to exclude any potential effect of anesthetics.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date July 10, 2017
Est. primary completion date July 10, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 80 Years
Eligibility <Healthy volunteers>

Inclusion Criteria:

- Age 20-45

- No underlying chronic disease

- Male volunteer

Exclusion Criteria:

- Under taking prescription drugs

- Taking herbal medicines within 2 weeks

- Baseline systolic blood pressure > 150 mmHg or diastolic pressure > 100 mmHg

- Body mass index < 18 kg/m^2 or > 30 kg/m^2

- Vigorous exercise, excessive alcohol, smoking or caffeine within 24 hours

- Any abnormalities on upper extremities

- Do not consent to participate

<Cardiac surgery patients>

Inclusion Criteria:

- Age 20-80

- Scheduled for cardiac surgery

Exclusion Criteria:

- Baseline systolic blood pressure > 150 mmHg or diastolic pressure > 100 mmHg

- Body mass index < 18 kg/m^2 or > 30 kg/m^2

- Uncontrolled diabetes

- Under taking beta-blockers

- Severe renal dysfunction, chronic kidney disease, on hemodialysis

- Any abnormalities on upper extremities (i.e, AV fistula on arms)

- Peripheral vascular disease, peripheral neuropathy, coagulopathy

- Vigorous exercise, excessive alcohol, smoking or caffeine within 24 hours

- Pregnant

- Emergency surgery

- Do not consent to participate

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ischemic conditioning
Four cycles of 5-min inflation of pneumatic cuff on upper extremity up to 200 mmHg, followed by 5-min deflation with no pressure.

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in microcirculation during ischemic conditioning Changes in occlusion slope during ischemia and recovery slope during reperfusion During 4-cycles of 5-min ischemia followed by 5-min reperfusion
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