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Swedish External Support Study

Swedish External Support Study is Randomized Trial of the Effect of External Support of PTFE-grafts for Bypass to Below Knee Arteries.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01273740
Acronym
SWEXSUS
Enrollment
334
Registered
2011-01-10
Start date
1995-01-31
Completion date
1998-06-30
Last updated
2011-01-10

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

Conditions

Critical Limb Ischemia

Keywords

PTFE bypass, femoro-popliteal, femoro-crural, popliteal arteries, crural arteries, external support, crtical limb ischemia

Brief 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.

Interventions

PROCEDUREExternal support

Bypass surgery with externally supported graft

Sponsors

Lasarettet Boden
CollaboratorOTHER
Borås Lasarett
CollaboratorOTHER
Eskilstuna Lasarettet
CollaboratorOTHER
Falu Lasarett Röntgen
CollaboratorOTHER
Department of Surgery, Sahlgrenska sjukhuset, Göteborg
CollaboratorUNKNOWN
Department of Surgery, Östra sjukhuset, Göteborg
CollaboratorUNKNOWN
Lasarett Gävle
CollaboratorOTHER
Helsingborgs Hospital
CollaboratorOTHER
Kalmar County Hospital
CollaboratorOTHER
Karlstad Central Hospital
CollaboratorOTHER
Kristiansund Hospital
CollaboratorOTHER
Lund University Hospital
CollaboratorOTHER
Malmö University
CollaboratorOTHER
Department of Surgery, Lasarettet, Motala
CollaboratorUNKNOWN
Department of Surgery, Lasarettet, Mölndal
CollaboratorUNKNOWN
Department of Surgery, Lasarettet, Norrköping
CollaboratorUNKNOWN
Department of Surgery, Lasarettet, Nyköping
CollaboratorUNKNOWN
Department of Surgery, Lasarettet, Skellefteå
CollaboratorUNKNOWN
Department of Surgery, Kärnsjukhuset, Skövde
CollaboratorUNKNOWN
Department of Surgery, S:t Görans Sjukhus, Stockholm
CollaboratorUNKNOWN
Department of Surgery, Södersjukhuset, Stockholm
CollaboratorUNKNOWN
Department of Surgery, Norra Älvsborgs Länssjukhus, Trollhättan-Vänersborg
CollaboratorUNKNOWN
Uppsala University Hospital
CollaboratorOTHER
Västervik Hospital
CollaboratorOTHER
Region Västmanland
CollaboratorOTHER
Department of Surgery, Lasarettet, Växjö
CollaboratorUNKNOWN
Department of Surgery, Lasarettet, Örebro
CollaboratorUNKNOWN
Department of Surgery, Lasarettet, Östersund
CollaboratorUNKNOWN
University Hospital, Linkoeping
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Critical limb ischemia Need for bypass surgery

Exclusion criteria

Can participate in follow-up Has suitable saphenous vein

Design outcomes

Primary

MeasureTime frame
primary graft patency

Secondary

MeasureTime frame
limb salvage

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026