Mechanochemical endovenous Ablation versus RADiOfrequeNcy Ablation in the treatment of primary great saphenous vein incompetence (MARADONA): study protocol for a randomized controlled trial

被引:23
|
作者
van Eekeren, Ramon R. J. P. [1 ]
Boersma, Doeke [2 ]
Holewijn, Suzanne [1 ]
Vahl, Anco [3 ,4 ]
de Vries, Jean Paul P. M. [2 ]
Zeebregts, Clark J. [5 ]
Reijnen, Michel M. P. J. [1 ]
机构
[1] Rijnstate Hosp, Dept Surg, NL-6815 AD Arnhem, Netherlands
[2] St Antonius Hosp, Dept Vasc Surg, NL-3435 CM Nieuwegein, Netherlands
[3] Onze Lieve Vrouw Hosp, Dept Surg, NL-1091 AC Amsterdam, Netherlands
[4] BovenIJ Hosp, Dept Surg, NL-1034 CS Amsterdam, Netherlands
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Vasc Surg, NL-9700 RB Groningen, Netherlands
来源
TRIALS | 2014年 / 15卷
关键词
Mechanochemical ablation; ClariVein; Radiofrequency ablation; Varicose vein; Therapy; Treatment; MOCA; Outcome; CHRONIC VENOUS DISEASE; VARICOSE-VEINS; CLINICAL-TRIAL; GENERAL-POPULATION; THERMAL ABLATION; EDINBURGH VEIN; LASER-ABLATION; INSUFFICIENCY; SURGERY; EPIDEMIOLOGY;
D O I
10.1186/1745-6215-15-121
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Radiofrequency ablation (RFA) is associated with an excellent outcome in the treatment of great saphenous vein (GSV) incompetence. The use of thermal energy as a treatment source requires the instillation of tumescence anesthesia. Mechanochemical endovenous ablation (MOCA) combines mechanical endothelial damage, using a rotating wire, with the infusion of a liquid sclerosant. Tumescence anesthesia is not required. Preliminary experiences with MOCA showed good results and low post-procedural pain. Methods/Design: The MARADONA (Mechanochemical endovenous Ablation versus RADiOfrequeNcy Ablation) trial is a multicenter randomized controlled trial in which 460 patients will be randomly allocated to MOCA or RFA. All patients with primary GSV incompetence who meet the eligibility criteria will be invited to participate in this trial. The primary endpoints are anatomic and clinical success at a one-year follow-up, and post-procedural pain. The secondary endpoints are technical success, complications, operation time, procedural pain, disease-specific quality of life, time taken to return to daily activities and/or work, and cost-efficiency analyses after RFA or MOCA. Both groups will be evaluated on an intention to treat base. Discussion: The MARADONA trial is designed to show equal results in anatomic and clinical success after one year, comparing MOCA with RFA. In our hypothesis MOCA has an equal anatomic and clinical success compared with RFA, with less post-procedural pain.
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页数:7
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