Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol

Bibliographic Details
Main Author: de Moraes Silva, Melissa Andreia
Publication Date: 2025
Other Authors: Fortes, Natália Leite, Oliveira, Luana de Andrade, Faria, Rodolfo Souza
Format: Article
Language: eng
Source: Revista Ciências em Saúde
Download full: https://portalrcs.hcitajuba.org.br/index.php/rcsfmit_zero/article/view/1469
Summary: Objective: To evaluate the effect of polidocanol foam sclerotherapy in patients with venous ulcers (VU) undergoing clinical treatment with elastocompression. Method: This will be a randomized, prospective, single-center, exploratory clinical trial with two parallel groups and 1:1 allocation. Participants aged 18-80 years with active VU and vascular Doppler ultrasound findings indicating chronic superficial venous insufficiency in both sexes will be included. Participants will be randomized into two groups: the Clinical group (undergoing conservative treatment with elastocompression) and Foam group (undergoing treatment of varicose veins with polidocanol foam associated with elastocompression). Thirty-four patients will be selected for each group. Participants in the Foam group will undergo superficial vein sclerotherapy using the Tessari technique, with the aid of ultrasound. Patients will be reassessed 30, 90, and 180 days after the intervention. The primary outcome will be lesion healing within 180 days. The secondary outcomes will be the VU healing time, rate of lesion area reduction, side effects, pain, quality of life (QOL) using the EQ-5D, and the Venous Clinical Severity Score. The data will be subjected to inferential tests and Kaplan-Meier survival analysis, assuming a significance level of 5%.
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spelling Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocolEffect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocolVaricose Veins, Sclerotherapy, Elastic Stockings, Varicose Ulcer, ProtocolObjective: To evaluate the effect of polidocanol foam sclerotherapy in patients with venous ulcers (VU) undergoing clinical treatment with elastocompression. Method: This will be a randomized, prospective, single-center, exploratory clinical trial with two parallel groups and 1:1 allocation. Participants aged 18-80 years with active VU and vascular Doppler ultrasound findings indicating chronic superficial venous insufficiency in both sexes will be included. Participants will be randomized into two groups: the Clinical group (undergoing conservative treatment with elastocompression) and Foam group (undergoing treatment of varicose veins with polidocanol foam associated with elastocompression). Thirty-four patients will be selected for each group. Participants in the Foam group will undergo superficial vein sclerotherapy using the Tessari technique, with the aid of ultrasound. Patients will be reassessed 30, 90, and 180 days after the intervention. The primary outcome will be lesion healing within 180 days. The secondary outcomes will be the VU healing time, rate of lesion area reduction, side effects, pain, quality of life (QOL) using the EQ-5D, and the Venous Clinical Severity Score. The data will be subjected to inferential tests and Kaplan-Meier survival analysis, assuming a significance level of 5%.Objective: To evaluate the effect of polidocanol foam sclerotherapy in patients with venous ulcers (VU) undergoing clinical treatment with elastocompression. Method: This will be a randomized, prospective, single-center, exploratory clinical trial with two parallel groups and 1:1 allocation. Participants aged 18-80 years with active VU and vascular Doppler ultrasound findings indicating chronic superficial venous insufficiency in both sexes will be included. Participants will be randomized into two groups: the Clinical group (undergoing conservative treatment with elastocompression) and Foam group (undergoing treatment of varicose veins with polidocanol foam associated with elastocompression). Thirty-four patients will be selected for each group. Participants in the Foam group will undergo superficial vein sclerotherapy using the Tessari technique, with the aid of ultrasound. Patients will be reassessed 30, 90, and 180 days after the intervention. The primary outcome will be lesion healing within 180 days. The secondary outcomes will be the VU healing time, rate of lesion area reduction, side effects, pain, quality of life (QOL) using the EQ-5D, and the Venous Clinical Severity Score. The data will be subjected to inferential tests and Kaplan-Meier survival analysis, assuming a significance level of 5%.Hospital de Clínicas de Itajubá2025-02-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPeer reviewedAvaliado pelos paresapplication/pdfhttps://portalrcs.hcitajuba.org.br/index.php/rcsfmit_zero/article/view/146910.21876/hsjhci.v15.e1469HSJ; Vol. 15 (2025); e1469HSJ; v. 15 (2025); e14692966-040810.21876/hsjhci.v15reponame:Revista Ciências em Saúdeinstname:Hospital de Clínicas de Itajubáinstacron:HCIenghttps://portalrcs.hcitajuba.org.br/index.php/rcsfmit_zero/article/view/1469/953Copyright (c) 2025 Melissa Andreia de Moraes Silva, Natália Leite Fortes, Luana de Andrade Oliveira, Rodolfo Souza Fariahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessde Moraes Silva, Melissa Andreia Fortes, Natália LeiteOliveira, Luana de AndradeFaria, Rodolfo Souza2025-03-01T11:29:23Zoai:ojs.portalrcs.hcitajuba.org.br:article/1469Revistahttps://portalrcs.hcitajuba.org.br/index.php/rcsfmit_zeroPUBhttps://portalrcs.hcitajuba.org.br/index.php/rcsfmit_zero/oaircs@hcitajuba.org.br||rcsfmit@medicinaitajuba.com.br2236-37852236-3785opendoar:2025-03-01T11:29:23Revista Ciências em Saúde - Hospital de Clínicas de Itajubáfalse
dc.title.none.fl_str_mv Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
title Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
spellingShingle Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
de Moraes Silva, Melissa Andreia
Varicose Veins, Sclerotherapy, Elastic Stockings, Varicose Ulcer, Protocol
title_short Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
title_full Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
title_fullStr Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
title_full_unstemmed Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
title_sort Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
author de Moraes Silva, Melissa Andreia
author_facet de Moraes Silva, Melissa Andreia
Fortes, Natália Leite
Oliveira, Luana de Andrade
Faria, Rodolfo Souza
author_role author
author2 Fortes, Natália Leite
Oliveira, Luana de Andrade
Faria, Rodolfo Souza
author2_role author
author
author
dc.contributor.author.fl_str_mv de Moraes Silva, Melissa Andreia
Fortes, Natália Leite
Oliveira, Luana de Andrade
Faria, Rodolfo Souza
dc.subject.por.fl_str_mv Varicose Veins, Sclerotherapy, Elastic Stockings, Varicose Ulcer, Protocol
topic Varicose Veins, Sclerotherapy, Elastic Stockings, Varicose Ulcer, Protocol
description Objective: To evaluate the effect of polidocanol foam sclerotherapy in patients with venous ulcers (VU) undergoing clinical treatment with elastocompression. Method: This will be a randomized, prospective, single-center, exploratory clinical trial with two parallel groups and 1:1 allocation. Participants aged 18-80 years with active VU and vascular Doppler ultrasound findings indicating chronic superficial venous insufficiency in both sexes will be included. Participants will be randomized into two groups: the Clinical group (undergoing conservative treatment with elastocompression) and Foam group (undergoing treatment of varicose veins with polidocanol foam associated with elastocompression). Thirty-four patients will be selected for each group. Participants in the Foam group will undergo superficial vein sclerotherapy using the Tessari technique, with the aid of ultrasound. Patients will be reassessed 30, 90, and 180 days after the intervention. The primary outcome will be lesion healing within 180 days. The secondary outcomes will be the VU healing time, rate of lesion area reduction, side effects, pain, quality of life (QOL) using the EQ-5D, and the Venous Clinical Severity Score. The data will be subjected to inferential tests and Kaplan-Meier survival analysis, assuming a significance level of 5%.
publishDate 2025
dc.date.none.fl_str_mv 2025-02-28
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer reviewed
Avaliado pelos pares
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://portalrcs.hcitajuba.org.br/index.php/rcsfmit_zero/article/view/1469
10.21876/hsjhci.v15.e1469
url https://portalrcs.hcitajuba.org.br/index.php/rcsfmit_zero/article/view/1469
identifier_str_mv 10.21876/hsjhci.v15.e1469
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://portalrcs.hcitajuba.org.br/index.php/rcsfmit_zero/article/view/1469/953
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital de Clínicas de Itajubá
publisher.none.fl_str_mv Hospital de Clínicas de Itajubá
dc.source.none.fl_str_mv HSJ; Vol. 15 (2025); e1469
HSJ; v. 15 (2025); e1469
2966-0408
10.21876/hsjhci.v15
reponame:Revista Ciências em Saúde
instname:Hospital de Clínicas de Itajubá
instacron:HCI
instname_str Hospital de Clínicas de Itajubá
instacron_str HCI
institution HCI
reponame_str Revista Ciências em Saúde
collection Revista Ciências em Saúde
repository.name.fl_str_mv Revista Ciências em Saúde - Hospital de Clínicas de Itajubá
repository.mail.fl_str_mv rcs@hcitajuba.org.br||rcsfmit@medicinaitajuba.com.br
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