OUTCOME OF PATIENTS ADMITTED WITH ACUTE LOWER EXTREMITY ISCHEMIA

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

176 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-03-04

Study Completion Date

2023-11-09

Brief Summary

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Acute ischemia of the lower limb (AMI) is a life-threatening emergency that threatens the functional prognosis of the limb. Depending on the clinical presentation and the anatomy of the patient, several therapeutic approaches can be considered: open surgery, endovascular surgery, hybrid surgery or amputation if revascularization is not feasible. The data in the current literature do not allow to clearly establish which therapeutic approach is the most adapted to the patient.

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Detailed Description

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Conditions

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Acute Ischemia of Lower Limb

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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patients with ischemia of the lower limbs

operation of ischemia of the lower limbs

Intervention Type PROCEDURE

The intervention technique is left to the judgment of the investigator to treat the ischemia

Interventions

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operation of ischemia of the lower limbs

The intervention technique is left to the judgment of the investigator to treat the ischemia

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Age greater than 18 years, regardless of gender.
* Diagnosis of AMI defined according to the Rutherford classification (2). AMI may involve one or both lower limbs.
* Be able to understand and give free and informed consent (non-opposition) to participate in the study
* To be affiliated to the social security system
* Not to object to participating in the study (collection of non-objection)

Exclusion Criteria

* Voluntary discharge of the patient: opposition to the use of the data (withdrawal of the non-objection)
* Termination of the study by decision of the sponsor or investigator.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No