Remote Ischemic Preconditioning Mechanism Study

EARLY_PHASE1CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

March 31, 2016

Study Completion Date

April 30, 2017

Conditions
Pain
Interventions
DEVICE

Remote Ischemic Preconditioning, Capsaicin, UV-B

The participants will have one disposable tourniquet applied to the left mid thigh by research personnel. The participants will then be randomized to the treatment group or sham group. The treatment group will receive 3 cycles of RIPC to the left lower leg by occluding blood flow at the thigh with a pneumatic cuff. Each cycle will consist of 5 minutes of ischemia by inflating the cuff to 300 mmHg followed by 5 minutes of reperfusion. The sham group will have the cuff inflated to no more than 15mmHg for three cycles as described above. Areas of hypersensitivity and allodynia will be obtained every 40 min for 280 min following the end of capsaicin application.

Trial Locations (1)

27157

WakeForestUBMC, Winston-Salem

All Listed Sponsors
lead

Wake Forest University Health Sciences

OTHER

NCT01541436 - Remote Ischemic Preconditioning Mechanism Study | Biotech Hunter | Biotech Hunter