UnknownNot Applicable

Post-operative Complication, Impulsive Compression, in Situ Bypass

Denmark100 participantsStarted 2018-02-08

Plain-language summary

To investigate whether compression therapy with foot pump reduce post-operative edema, facilitate wound healing of operation wounds, promote healing of ischemic ulcers and shorten hospitalization, increase and improve the patient's subjective quality of life faster

Who can participate

Age range18 Years – 99 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Patients who need an insitu bypass from Common Femoral Artery to Popliteal AK/BK or crural Artery Exclusion Criteria: Ischemic wound that are located in such manner that compression of the foot is not possible. Former deep vein trombosis (DVT) or symptomatic post thrombotic syndrome (PTS) We only include patients without any connections to other studies-

What they're measuring

Reduction of wound complications in the foot pump group

Timeframe: From randomization until 12 month examination (individual finish examination)

Trial details

NCT IDNCT03192982

SponsorKolding Sygehus

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-11-28

Contact for this trial

Hans Ravn, MD PhD

004528718505 hans.ravn@rsyd.dk

View on ClinicalTrials.gov More Compresion Therapy trials