Swedish External Support Study

NCT01273740 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 334

Last updated 2011-01-10

No results posted yet for this study

Summary

Randomized study to evaluate the effect of adding external support to PTFE-grafts used for bypass to below knee arteries in patients with critical limb ischemia with respect to primary patency, secondary patency, and limb salvage.

Conditions

  • Critical Limb Ischemia

Interventions

PROCEDURE

External support

Bypass surgery with externally supported graft

Sponsors & Collaborators

  • Lasarettet Boden

    collaborator OTHER
  • Borås Lasarett

    collaborator OTHER
  • Eskilstuna Lasarettet

    collaborator OTHER
  • Falu Lasarett Röntgen

    collaborator OTHER
  • Department of Surgery, Sahlgrenska sjukhuset, Göteborg

    collaborator UNKNOWN
  • Department of Surgery, Östra sjukhuset, Göteborg

    collaborator UNKNOWN
  • Lasarett Gävle

    collaborator OTHER
  • Helsingborgs Hospital

    collaborator OTHER
  • Kalmar County Hospital

    collaborator OTHER
  • Karlstad Central Hospital

    collaborator OTHER
  • Kristiansund Hospital

    collaborator OTHER
  • Lund University Hospital

    collaborator OTHER
  • Malmö University

    collaborator OTHER
  • Department of Surgery, Lasarettet, Motala

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Mölndal

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Norrköping

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Nyköping

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Skellefteå

    collaborator UNKNOWN
  • Department of Surgery, Kärnsjukhuset, Skövde

    collaborator UNKNOWN
  • Department of Surgery, S:t Görans Sjukhus, Stockholm

    collaborator UNKNOWN
  • Department of Surgery, Södersjukhuset, Stockholm

    collaborator UNKNOWN
  • Department of Surgery, Norra Älvsborgs Länssjukhus, Trollhättan-Vänersborg

    collaborator UNKNOWN
  • Uppsala University Hospital

    collaborator OTHER
  • Västervik Hospital

    collaborator OTHER
  • Region Västmanland

    collaborator OTHER
  • Department of Surgery, Lasarettet, Växjö

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Örebro

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Östersund

    collaborator UNKNOWN
  • University Hospital, Linkoeping

    lead OTHER

Principal Investigators

  • Fredrik BG Lundgren, PhD, MD · Department of CardioVascular Surgery, University Hospital, Linköping, Sweden

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1995-01-31
Primary Completion
1998-06-30
Completion
1998-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01273740 on ClinicalTrials.gov