NCT01230567

Brief Summary

50 patients with non healing wounds will undergo biopsy to conclude wether there is an occult etiology for the wound.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
41

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Oct 2010

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

October 1, 2010

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

October 28, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 29, 2010

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2012

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2013

Completed
Last Updated

April 10, 2013

Status Verified

April 1, 2013

Enrollment Period

2.2 years

First QC Date

October 28, 2010

Last Update Submit

April 9, 2013

Conditions

Wounds and Injuries

Keywords

Problem woundsNon healing woundsBCCSCCVasculitis

Outcome Measures

Primary Outcomes (1)

  • HISTOLOGY RESULTS

    HISTOLOGY RESULTS OF ALL WOUND BIOPSIES WILL BE COLLECTED TO ASSESS THE ACCULT ETIOLOGY RATE IN NON HEALING WOUNDS.

    04/2013

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients suffering from non healing wounds, which do not respond well to six weeks of adequate treatment.

You may qualify if:

  • patients with non-healing wounds (for \> 6 weeks)
  • consent to be included in the study
  • age 18-85

You may not qualify if:

  • patients taking anti coagulant therapy
  • patients taking steroids or immunosuppressive therapy
  • pregnancy
  • pace maker

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Carmel Medical Center

Haifa, 34362, Israel

Location

MeSH Terms

Conditions

Wounds and InjuriesVasculitis

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular Diseases

Study Officials

  • Yaron Har-Shai, Prof

    Carmel Medical Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
head of plastic surgery department

Study Record Dates

First Submitted

October 28, 2010

First Posted

October 29, 2010

Study Start

October 1, 2010

Primary Completion

December 1, 2012

Study Completion

April 1, 2013

Last Updated

April 10, 2013

Record last verified: 2013-04

Locations

IL(1)