Prolonged Cryocompression and Skin Temperature: a Safety and Feasibility Pilot

NACompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

February 12, 2025

Primary Completion Date

May 30, 2025

Study Completion Date

May 30, 2025

Conditions
Skin Temperature ChangeAdverse EffectsSafety of InterventionCryotherapyFeasibility Pilot Study
Interventions
DEVICE

Prolonged (2-hour) cryocompression therapy

The cuff of the device will be attached around the knee randomised to receive the treatment as per the manufacturer's instruction. Then the device will be set to apply a standard 30-minute treatment with a temperature of 8 ℃ and intermittent compression of 25-50 mmHg. Following this, and depending on the randomised condition, the treatment will continue for a further 90-minutes with a temperature of either 10 ℃ or 12 ℃ being applied by the device. The level of compression will remain the same (25-50 mmHg) throughout all tests.

Trial Locations (1)

SO22 4NR

University of Winchester, Winchester

Sponsors
All Listed Sponsors
collaborator

Physiolab Technologies Ltd

INDUSTRY

lead

University of Winchester

OTHER

NCT06673277 - Prolonged Cryocompression and Skin Temperature: a Safety and Feasibility Pilot | Biotech Hunter | Biotech Hunter