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Active, not recruiting Observational

Clinical Outcomes Following Surgical Debridement of Diabetic Foot Infection with Borderline Vascularity

NCT05553509 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2023-01-01
Last updated
2024-11-26

Condition(s) studied

Chronic Limb Threatening Ischemia

Investigational drug(s) / intervention(s)

PER CUTANEOUS TRANSLUMINAL ANGIOPLASTY

PER CUTANEOUS TRANSLUMINAL ANGIOPLASTY: SURGICAL DEBRIDEMNT

Study summary

Observe Timing to complete healing of wounds \& Limb salvage in both cohorts those who are undergoing Debridement only and those who are undergoing Debridement plus PTA

Eligibility

Sex
ALL
Min age
30 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients will be included in this study are those suffering from DFUs; and Borderline Ischemia (BLI) / Borderline Vacularity with (Rutherford Grade "I" Categories "2\&3") when they have a borderline ankle systolic pressure Exclusion Criteria: * All patients with (CLI) and DFUs as they are indicated for urgent re-vascularization. Severely infected/ gangrenous wounds requiring amputation hindering possible limb salvage. Lesions lying within or adjacent to an aneurysm; Non diabetic cases with foot ulcers; Arteritic lesions;(Vasculitic Patients). Patients had prior major amputation, bypass surgery, and endarterectomy on any vessel of the ipsilateral (target) extremity

Primary outcome measure(s)

  • Clinical Outcomes Following Surgical Debridement of Diabetic Foot Infection With Borderline Vascularity — 1 YEAR
    1. Observe the timing to complete wound healing in both cohorts those with Debridement only \& those with Debridment plus PTA 2. Observe the Rate of limb salvage in both groups

Trial sites (1)

FacilityCityRegionStatus
Department of vascular surgery - Assiut University Hospital Asyut Asyut Governorate
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05553509 on ClinicalTrials.gov ↗ ← All trials in Egypt