Varicose Veins Clinical Trial
Official title:
A Randomised Controlled Trial Comparing Duration of Compression Hosiery After Endovenous Ablation of Varicose Veins
Compression stockings are traditionally worn for a period of time after varicose vein surgery
to reduce pain and bruising. The investigators provide an ambulatory endovenous ablation
service. Patients come to the Veins Unit, receive oral sedation, have their veins treated
with either laser or radiofrequency ablation plus phlebectomies* under local anaesthetic,
recover for an hour and then go home. *Phlebectomy describes the technique of pulling out
small varicose veins through small incisions in the overlying skin. The standard practice of
the Veins Unit is to advise patients to wear class two compression stockings for four weeks
post-operatively. Many patients would prefer a shorter period of time in stockings.
The Nice Guidelines for Varicose Veins has posed the question: 'How long should stockings be
worn for after endovenous ablation?'
Three trials have addressed this issue:
Bakker looked at patients who wore stockings for either two or seven days after laser
ablation only; the group who wore stockings for seven days fared better.
Elderman looked at patients who either wore no stockings or stockings for two weeks after
laser ablation only; the group who wore stockings for two weeks had less pain.
Krasznai looked at patients who wore stockings for either 4 hours or 72 hours after
radiofrequency ablation only; there was no significant difference in post-op pain among
groups.
None of these trials included patients who had phlebectomies at the same time. This study
aims to answer the question 'How long is it necessary to wear compression stockings for after
endovenous ablation (either laser or radiofrequency) plus concomitant phlebectomies?' The
investigators plan to divide 110 patients into two groups- either 'stockings for 2 weeks'
(trial group) or 'stockings for 4 weeks' (usual treatment group).
Pre-operatively, all patients will fill out a pain score and two short quality of life
questionnaires, one specific to varicose veins. Post-operatively at home, all patients will
be asked to keep a diary of pain and analgesia use. They will also document bruising at seven
days on charts and on a visual scale. At their four week clinic review, all patients will be
asked to fill out a pain and bruising score, a bruising chart and the two short quality of
life questionnaires again.
The group with the best pain, bruising and quality of life scores post-operatively will help
guide duration of compression therapy for future patients.
The Nice Guidelines for Varicose Veins, published by the NHS in 2013, questioned the clinical
benefit of stockings after endovenous ablation, and if there is benefit, how long the
stockings should be worn for.
Three randomised controlled trials have addressed these issues:
Bakker and colleagues randomised 69 patients into two groups- stockings were worn for either
two or seven days after laser ablation. The group who wore stockings for seven days had
better pain and quality of life scores.
Elderman and colleagues randomised 111 patients who had laser ablation into two groups- a
group who wore no stockings, or a group who wore stockings for two weeks. The group who wore
stockings for two weeks had less pain and required less analgesia.
Krasznai and colleagues randomised 101 patients into two groups- stockings were worn for
either 4 hours or 72 hours after radiofrequency ablation only; there was no significant
difference in post-op pain among groups.
None of these trials included patients who had phlebectomies at the same time.
This study hopes to answer the question 'How long is it necessary to wear compression
stockings for after endovenous ablation (either laser or radiofrequency) plus concomitant
phlebectomies?'
110 consecutive patients will be randomised into 'stockings for 2 weeks' (trial group) or
'stockings for 4 weeks' (usual treatment group). Randomisation will be facilitated by online
random number generation (https://www.random.org/). Patients with odd numbers will be
allocated into the trial group; those randomly assigned even numbers will be allocated into
the usual treatment group.
Pre-operatively, all patients will be asked to fill out a visual analog pain score (VAS), the
Aberdeen Varicose Veins questionnaire and the RAND 36-Item Health Survey. Patients will be
evaluated in terms of CAEP staging and the Venous Clinical Severity Score (VCSS) by the
supervising nurse or physician.
Endovenous laser therapy (EVLT) plus phlebectomies or radiofrequency ablation (RFA) plus
phlebectomies will be performed in the standard manner.
The trial group will wear the stockings for 24 hours a day for the first 4 days, and then
during the day only for the next 10 days. The usual treatment group will wear the stockings
for 24 hours a day for a week, and then during the day only for the next 3 weeks.
Post-operatively at home, patients will be asked to keep a diary of pain and analgesia use.
They will also document bruising at 7 days on a diagram and on a visual analog scale.
At their 4 week clinic review, again the VCSS will completed and patients will be asked to
fill out a visual analog pain and bruising score, a bruising diagram, the Aberdeen Varicose
Veins questionnaire and the RAND 36-Item Health Survey.
Primary outcome measures are post-operative pain scores on the visual analog scale and
post-operative bruising scores on the visual analog scale.
Secondary outcome measures are changes in veins-related quality of life measured on the
Aberdeen Varicose Veins Questionnaire and changes in overall quality of life based on the
RAND 36-Item Health Survey.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02441881 -
Trial of Radiofrequency Thermo-ablation Treatments of Great Saphenous Varicose Veins (3-RF Study)
|
N/A | |
Completed |
NCT03283800 -
Copper Impact on Venous Insufficiency and Lipodermatosclerosis
|
N/A | |
Withdrawn |
NCT01203397 -
Safety And Efficacy Study Of Topic Mucopolysaccharide Polysulfate In The Superficial Varicose Veins Treatment
|
Phase 3 | |
Withdrawn |
NCT01426035 -
Safety And Efficacy Study Of Topic Mucopolysaccharide Polysulfate Cream In The Superficial Varicose Veins Treatment
|
Phase 3 | |
Recruiting |
NCT02054325 -
Study Protocol Comparing Polidocanol Versus Hypertonic Glucose for Treatment of Reticular Veins
|
Phase 4 | |
Withdrawn |
NCT03601572 -
Hypnoanalgesia in Surgical and Endovenous Treatment of Varicosis
|
||
Completed |
NCT04933591 -
Impact of Treatment With VENARUS® on the Level of Monocyte Chemoattractant Protein 1 in Varicose Veins Blood
|
N/A | |
Active, not recruiting |
NCT02397226 -
Lower Limb Venous Insufficiency and the Effect of Radiofrequency Treatment Versus Open Surgery
|
N/A | |
Withdrawn |
NCT02936271 -
Efficacy of Vasculera in Prevention on Post-op Pain and Edema Following Lower Extremity Venous Treatment in the Outpatient Setting
|
N/A | |
Terminated |
NCT02557542 -
Pilot RCT Evaluating a One Stop Vein Clinic
|
N/A | |
Completed |
NCT00758420 -
Randomized, Single Blind, Placebo Controlled, to Evaluate Efficacy and Safety of Polidocanol Injectable Foam for Treatment of Symptomatic, Visible Varicose Veins With SFJ Incompetence
|
Phase 2/Phase 3 | |
Active, not recruiting |
NCT00841178 -
Endovenous Laser Therapy (EVLT) for Sapheno-Popliteal Incompetence and Short Saphenous Vein (SSV) Reflux: A RCT
|
N/A | |
Not yet recruiting |
NCT05508581 -
Microwaves Ablation of Varicose Veins
|
N/A | |
Completed |
NCT05247333 -
Implementation of a Minor Ailment Service in Community Pharmacy Practice
|
N/A | |
Active, not recruiting |
NCT04339075 -
Registry to Investigate the Efficacy and Safety of VenaBlock VeIn SEaling System for VaRicose Veins in SingApore
|
||
Completed |
NCT03392753 -
Mechanochemical Ablation Compared to Cyanoacrylate Adhesive
|
N/A | |
Recruiting |
NCT04146168 -
Lake Washington Vascular VenaSealâ„¢ Post-Market Evaluation
|
||
Recruiting |
NCT02304146 -
Long-term Ultrasound Guided Foam Sclerotherapy Versus Classical Surgical Stripping Study
|
N/A | |
Completed |
NCT01231373 -
Polidocanol Endovenous Microfoam (PEM) Versus Vehicle for the Treatment of Saphenofemoral Junction (SFJ) Incompetence
|
Phase 3 | |
Completed |
NCT01200199 -
Validity of Electronic Diary for Monitoring Varicose Veins Symptoms
|