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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04036734
Other study ID # USGSV
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 24, 2019
Est. completion date March 1, 2020

Study information

Verified date March 2020
Source National University of Ireland, Galway, Ireland
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Longitudinal ultrasound orientation during central venous cannulation has been suggested by a number of radomised studies to offer superior cannulation rates. This technique may offer a simple, safe and cost-neutral step to improve cannulation rates in the widely performed minimally invasive endovenous intervention.


Description:

Varicose veins are an extremely common disorder and negatively impact on patient quality of life. In recent years minimally invasive venous treatments for varicose veins (MIVT) have emerged as an effective alternative to open surgery. It is associated with a reduction in peri-operative morbidity, recovery time and increased quality of life scores when compared with open surgical stripping4. Furthermore, MIVT is now widely carried out under local anaesthesia.

Typically, MIVT requires cannulation, under ultrasound guidance, of either the great or small saphenous vein in the lower extremity to allow subsequent passage of a venous catheter. This cannulation technique is widely used for venous and arterial cannulation throughout the body. It entails utilising an ultrasound probe in either a longitudinal or transverse orientation (to the target vein) to guide an entry needle into a target vessel. The longitudinal orientation, while unstable, offers better visualisation of the vein when performed accurately. Conversely, the transverse approach is very stable with poorer visualisation of the target vessel. As such, no definitve guidance is available to guide treating physicians as to the optimal orientation with a wide variation among practitioners.

The cannulation process for MIVT is often further challenged by both the small calibre and tendency toward vasospasm of target veins. Failure of cannulation may result in greater rates of conversion to open surgery exposing the patient to the the higher rate of morbidity associated with open surgery. More importantly, repeated cannulation results in significant discomfort and hence a reduction in patient satisfaction.

Longitudinal ultrasound orientation during venous cannulation has been suggested by a number of radomised studies to offer superior cannulation rates of cannulation. This technique may offer a simple, safe and cost-neutral step to improve cannulation rates in the widely performed MIVT.

The authors propose a blinded randomized controlled study to investigate the effects of ultrasound orietation on cannulation rates in MIVT. To test this hypothesis we plan to randomise 100 patients undergoing MIVT to either venous cannulation with transverse or longitudinal orientation of the ultrasound probe.


Recruitment information / eligibility

Status Completed
Enrollment 101
Est. completion date March 1, 2020
Est. primary completion date March 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- For minimally invasive venous surgery of the lower limb (Clinical-Etiology-Anatomy-Pathophysiology (CEAP) classification score 2 of greater)

- Intervention requiring venous cannulation of axial lower limb vein

- Full consent

- >18 years

- No concomitant deep venous incompetence

Exclusion Criteria:

- General anaesthesia

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Longitudinal
Longitudinal orientation of ultrasound to long axis of vein to guide access needle
Transverse
Transverse orientation of ultrasound to long axis of vein to guide access needle

Locations

Country Name City State
Ireland Saolta University Hospital Group Galway

Sponsors (1)

Lead Sponsor Collaborator
National University of Ireland, Galway, Ireland

Country where clinical trial is conducted

Ireland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall successful Cannulation rate as a percentage Overall successful cannulation of the target axial lower limb vein for endovenous treatment. Successful cannulation will be defined as intraluminal placement of the access cannula in the targeted axial vein. Immediate
Secondary Time in seconds to cannulation Time from skin puncture to successful placement of access catheter in the target vein Immediate
Secondary Number of cannulation attempts Number of times the skin is pierced in an attempt to cannulate the target vein Immediate
Secondary Peri-cannulation pain Pain will be measured using a visual analogue scale of 0-100 Immediate
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