Effect of polidocanol foam sclerotherapy for the treatment of venous ulcers: a randomized clinical trial protocol
Main Author: | |
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Publication Date: | 2025 |
Other Authors: | , , |
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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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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1831507754460643328 |