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Recruiting NCT05030259

The Research About the ACS After Femoropopliteal Arterial Injuries

— Observational Acute Compartment Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: fasciotomy.
Who it may be relevant to
Registry conditions: Acute Compartment Syndrome. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

ACS After Femoropopliteal Arterial Injuries

Overview

Crural Compartment syndrome is a well-known sequela after femoropopliteal arterial injuries in the lower extremity, particularly when there has been a long period of ischemia,need for ligation of a major vein, or when there is severe associated soft tissue.There is conteoversy in the treatment.

Interventions

  • Procedure fasciotomy
    To perform fasciotomy

Primary outcome measures

  • the rate of amputation [Time frame: up to 6 months]
  • fasciotomy performed or not [Time frame: up to 2 weeks]
Secondary outcome measures (12)
  • the rate of primary skin closure [Time frame: up to 1 months]
  • hospital lengths of stay [Time frame: up to 6 months]
  • injury mechanism of patients [Time frame: up to 1 week]
  • the costs of hospitalization [Time frame: up to 2 months]
  • tourniquet used or not [Time frame: up to 1 week]
  • the time of using tourniquet [Time frame: up to 1 week]
  • the time to surgical intervention [Time frame: up to 1 month]
  • extremity Abbreviated Injury Scale of patients [Time frame: up to 1 week]
  • Injury Severity Score of patients [Time frame: up to 1 week]
  • concomitant injury of patients [Time frame: up to 1 week]
  • time of skin closure [Time frame: up to 1 month]
  • admission hemoglobin of patients [Time frame: up to 1 month]

Eligibility criteria

Inclusion criteria

  • patients with femoropopliteal arterial injuries
  • patients older than 18 years

Exclusion criteria

  • Patients who did not survive to discharge
  • Patients with primary amputation
  • patients younger than 18 years

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • the Third Hospital of Hebei Medical Univesity — Shijiazhuang

Identifiers

NCT: NCT05030259 · HZY005ACS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗