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Sequential Compression Devices Effect on Fibrinolysis in Plastic Surgery Outpatients

NCT03821597 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2019-01-31

No results posted yet for this study

Summary

This study investigates a possible fibrinolytic effect of sequential compression devices (SCDs). These devices have been used for decades to reduce risk of deep venous thrombosis (DVT). However, a randomized study in plastic surgery outpatients has not been done. This study is undertaken to remedy that deficiency in our knowledge base.

Conditions

  • Blood Coagulation Disorder

Interventions

PROCEDURE

Sequential compression devices (SCDs)

Application of sequential compression devices in surgery.

PROCEDURE

No sequential compression.

No sequential compression devices are applied.

Sponsors & Collaborators

  • Swanson Center

    lead OTHER

Principal Investigators

  • Eric Swanson, M.D. · Swanson Cener

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-11-01
Primary Completion
2018-12-31
Completion
2019-01-27

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03821597 on ClinicalTrials.gov