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Comparison of therapeutic results of large vein harvesting with conventional / small incisions for lower limb vascular repair in patients with chronic lower limb ischemia

Comparison of therapeutic results from great saphenous vein harvesting with conventional and standard bridging techniques for lower limb revascularization in patients with chronic lower limb ischemia

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190511043562N1
Enrollment
60
Registered
2019-11-05
Start date
2019-11-05
Completion date
Unknown
Last updated
2019-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic lower limb ischemia. Unspecified disorder of circulatory system

Interventions

Intervention 1: Intervention group: Removal of large saphenous vein by bridging method (multiple and small incisions), the skin incision starts from the groin area and is created by a 4cm skin bridgin

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 18 years and older Patients Candidate for Lower Limb Vascular Reconstruction Using Self-Patient Large Saphenous Vein (Autolog) Patients with consent to participate in the study

Exclusion criteria

Exclusion criteria: Patients with susceptible to bleeding Coagulation Disorders Immune system disorder Long-term use of steroids to reduce the incidence of postoperative complications History of harvesting of both saphenous veins History of limb saphenectomy Edema caused by systemic diseases Inferior venous insufficiency Patients with no consent to participate in the study

Design outcomes

Primary

MeasureTime frame
Pain level. Timepoint: Daily during the hospitalization , and 1,3,6 months after surgery. Method of measurement: Visual analog scale (0= None, 1-3 Mild, 4-7 Moderate, 8-10 severe).;Graft patency. Timepoint: 1,3, and 6 months after surgery. Method of measurement: Physician examination.

Secondary

MeasureTime frame
Results of surgery. Timepoint: 1,3, and 6 months after surgery. Method of measurement: Physical examination.;Postoperative complications (infection, dehiscence, hematoma, scar after surgery). Timepoint: 1,3, and 6 months after surgery. Method of measurement: Physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactIraj Nazari MD.

Ahvaz University of Medical Sciences

nazari-i@ajums.ac.ir+98 61 3374 3001

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026