Scandinavian Miller Collar Study

NCT01285986 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 352

Last updated 2011-01-28

No results posted yet for this study

Summary

Randomized study to evaluate the effect of adding a vein collar at the distal anastomosis 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

Vein collar at the distal anastomosis

Vein collar interposed at the distal anastomosis or No vein collar interposed at the distal anastomosis

Sponsors & Collaborators

  • Sunderbyn Hospital

    collaborator OTHER
  • Borås Lasarett

    collaborator OTHER
  • Eskilstuna Lasarettet

    collaborator OTHER
  • Falu Lasarett Röntgen

    collaborator OTHER
  • Sahlgrenska University Hospital

    collaborator OTHER
  • 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, Sweden

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Mölndal, Sweden

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Norrköping, Sweden

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Nyköping, Sweden

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Skellefteå, Sweden

    collaborator UNKNOWN
  • Department of Surgery, Kärnsjukhuset, Skövde, Sweden

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

    collaborator UNKNOWN
  • Department of Surgery, Södersjukhuset, Stockholm, Sweden

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

    collaborator UNKNOWN
  • Uppsala University Hospital

    collaborator OTHER
  • Västervik Hospital

    collaborator OTHER
  • Region Västmanland

    collaborator OTHER
  • Department of Surgery, Lasarettet, Växjö, Sweden

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Örebro, Sweden

    collaborator UNKNOWN
  • Department of Surgery, Lasarettet, Östersund, Sweden

    collaborator UNKNOWN
  • Department of Vascular Surgery, Sykehuset, Kolding, Denmark

    collaborator UNKNOWN
  • Rigshospitalet, Denmark

    collaborator OTHER
  • Aalborg University Hospital

    collaborator OTHER
  • University Hospital, Linkoeping

    lead OTHER

Principal Investigators

  • Fredrik BG Lundgren, MD, PhD · 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

Countries

  • Sweden

Study Locations

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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 NCT01285986 on ClinicalTrials.gov