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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01195623
Other study ID # ETKI 96-169
Secondary ID
Status Completed
Phase N/A
First received September 3, 2010
Last updated February 13, 2013
Start date November 1997
Est. completion date August 2010

Study information

Verified date February 2013
Source Uppsala University Hospital
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Interventional

Clinical Trial Summary

Duplex imaging is costly and time-consuming, but is used increasingly for preoperative evaluation of varicose veins. Its value in terms of the long-term results of surgery is not clear. 293 patients (343 limbs) with primary varicose veins were randomized to operation with or without preoperative duplex imaging. Reoperation rates, clinical and duplex findings were compared at 2 months and 2 years after surgery. Routine preoperative duplex examination led to an improvement in results. However two years is a short time, and with a longer follow-up other mechanisms for recurrence may become more important, e.g. neovascularization (new vessel formation) or progression of disease, hence the value of a detailed preoperative diagnosis may be diminished. The aim of this phase of the investigation is to study the results after 8 years, in particular what mechanisms for recurrences were most important.


Recruitment information / eligibility

Status Completed
Enrollment 293
Est. completion date August 2010
Est. primary completion date September 2003
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria:

- patients with primary varicose veins

Exclusion Criteria:

- pure cosmetic complaints

- previous venous surgery or sclerotherapy

- history of suspect or manifest deep venous thrombosis

- active or healed venous ulceration

- peripheral arterial disease

- previous significant trauma to the leg

- general illness

- alcohol or drug abuse

- unable to understand information

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
preoperative duplex examination

Preoperative duplex


Locations

Country Name City State
Sweden Capio StGörans Gospital Stockholm

Sponsors (3)

Lead Sponsor Collaborator
Uppsala University Hospital Capio Research Foundation, Stockholm County Council, Sweden

Country where clinical trial is conducted

Sweden, 

References & Publications (4)

Blomgren L, Johansson G, Bergqvist D. Quality of life after surgery for varicose veins and the impact of preoperative duplex: results based on a randomized trial. Ann Vasc Surg. 2006 Jan;20(1):30-4. — View Citation

Blomgren L, Johansson G, Bergqvist D. Randomized clinical trial of routine preoperative duplex imaging before varicose vein surgery. Br J Surg. 2005 Jun;92(6):688-94. — View Citation

Blomgren L, Johansson G, Dahlberg-Akerman A, Thermaenius P, Bergqvist D. Changes in superficial and perforating vein reflux after varicose vein surgery. J Vasc Surg. 2005 Aug;42(2):315-20. — View Citation

Blomgren L, Johansson G, Emanuelsson L, Dahlberg-Åkerman A, Thermaenius P, Bergqvist D. Late follow-up of a randomized trial of routine duplex imaging before varicose vein surgery. Br J Surg. 2011 Aug;98(8):1112-6. doi: 10.1002/bjs.7579. Epub 2011 May 27. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of Re-do Surgery number of reoperations (legs) in the two treatment arms 7 years mean No
Secondary Recurrence Rate number of recurrences in treatment arms but also nature of recurrences 7 years No
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