Role of Adiponectine in Pathophysiology Ogf Diabetic Foot
1 other identifier
observational
70
0 countries
N/A
Brief Summary
Diabetic patients with a history of diabetic foot are considered to be a high-risk population for increased cardiovascular and all-cause mortality (1,2,3,). Diabetic foot (DF) is responsible for more hospitalizations than any other complication of diabetes and are the leading cause of non-traumatic lower extremity amputations, resulting in nearly 100 000 amputations annually in the US alone (4,5,6). Surgical debridement, as an important component of standard of care of diabetic foot, is intended to remove healing-impaired tissue, decreases bacterial burden, thus to stimulate overall wound closure, while removing as little of healing-competent skin as possible. Furthermore, debrided tissue is often used as a valuable tissue source for research purposes (7,8,9,10). Debrided tissue presents valuable diagnostic and research source to verify pathology, assess prognosis and gain insights into DF molecular pathology, all of which ultimately leads to improved outcomes. We aimed to validate tissue obtained from surgical debridement of DF for the cellular/molecular tissue analyses and biomarkers, to evaluate the pathophysiology of DF and understanding mechanisms that inhibit healing. The age range will be 50-70 years, in order to minimize the effects of irreversible vascular wall changes induced progressively by the aging process. All patients will undergo screening procedures that will include full anamnesis, physical examination, basic laboratory blood tests (full chemistry, CBC); urine examination and EKG will be performed at start and at the end of the study. Patients with a significant myocardial, and renal, cerebrovascular or hepatic disease will be excluded from the study. In a prospective study, we will collect wound edge tissue specimens from 75 patients with DF during surgical debridement. From each patient, 1-4 specimens will be obtained per debridement. To evaluate debrided tissue, each specimen will be processed for paraffin embedding and stained with haematoxylin and eosin. Histopathology analysis of multiple specimens acquired from the same wound will be analysed.
Trial Health
Trial Health Score
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participants targeted
Target at P25-P50 for all trials
Started Feb 2015
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 20, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2017
CompletedFirst Submitted
Initial submission to the registry
May 10, 2017
CompletedFirst Posted
Study publicly available on registry
May 12, 2017
CompletedMay 12, 2017
March 1, 2017
12 months
May 10, 2017
May 11, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
dIABETIC FOOT ULCERS INCIDENCE
1 year
Study Arms (1)
diabetic patients
In a prospective study, we will collect wound edge tissue specimens from 75 patients with DF during surgical debridement. From each patient, 1-4 specimens will be obtained per debridement. To evaluate debrided tissue, each specimen will be processed for paraffin embedding and stained with haematoxylin and eosin. Histopathology analysis of multiple specimens acquired from the same wound will be analysed. Full-thickness epidermis biopsies will be followed by biomarker assessment such as: 1. Expression of insulin-like growth factor 1 receptor (IGF-1R) 2. Adiponectin 3. Leptin 4. Resistin 5. Osteocalcin 6. Osteoprotegerin 7. Insulin, c-peptid 8. HOMA-IR
Interventions
Eligibility Criteria
diabetic patients hospitalized from January 2015 through December 2016 in Wolfson Medical Center due to the diagnosis of diabetic foot
You may qualify if:
- patients hospitalized from January 2015 through December 2016 in Wolfson Medical Center due to the diagnosis of diabetic foot
You may not qualify if:
- Patients with a history of unstable angina, MI, CVA or major surgery within the six months preceding entrance to the study were excluded.
- Patients with unbalanced endocrine disease were excluded, as were patients with plasma creatinine \> 2.5 mg/dl and elevation of liver enzymes to more than twice the upper normal limit.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Shargorodsky MARINA
Study Record Dates
First Submitted
May 10, 2017
First Posted
May 12, 2017
Study Start
February 20, 2015
Primary Completion
February 1, 2016
Study Completion
February 1, 2017
Last Updated
May 12, 2017
Record last verified: 2017-03