NCT04672668

Brief Summary

in our study we are examining the volume flow of the common femoral artery before and after angigraphy of a critical ischemic limb, as a predictor for wound healing after the treatment

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2020

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 13, 2020

Completed
Same day until next milestone

Study Start

First participant enrolled

December 13, 2020

Completed
4 days until next milestone

First Posted

Study publicly available on registry

December 17, 2020

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2021

Completed
2.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

February 20, 2024

Completed
Last Updated

December 17, 2020

Status Verified

December 1, 2020

Enrollment Period

1 year

First QC Date

December 13, 2020

Last Update Submit

December 13, 2020

Conditions

Outcome Measures

Primary Outcomes (1)

  • wound healing

    physical examination

    12 months

Interventions

duplex ultrasound for the common femoral artery before and after the angiography

Eligibility Criteria

Age12 Years - 120 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients with threatened limbs, having angioplasty .

You may qualify if:

  • All patients with threatened limbs, that was decided upon to have angioplasty .

You may not qualify if:

  • those who are not willing to sign a consent form to participate in this study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sheba Health Center

Ramat Gan, Israel

Location

MeSH Terms

Interventions

Ultrasonography, Doppler, Duplex

Intervention Hierarchy (Ancestors)

Ultrasonography, DopplerUltrasonographyDiagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

Study Officials

  • moshe halak, dr

    sheba health center

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Target Duration
12 Months
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
dr

Study Record Dates

First Submitted

December 13, 2020

First Posted

December 17, 2020

Study Start

December 13, 2020

Primary Completion

December 30, 2021

Study Completion

February 20, 2024

Last Updated

December 17, 2020

Record last verified: 2020-12

Data Sharing

IPD Sharing
Will not share

Locations