Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)

Detalhes bibliográficos
Autor(a) principal: Souza, Gustavo H.B.
Data de Publicação: 2012
Outros Autores: Maistro, Edson L. [UNESP], Rodrigues, Marcelo, Carvalho, Jose C.T., Fonseca, Fernando L.A., Lopes, Andrey P., Perazzo, Fabio F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/226727
Resumo: Painful bladder syndrome associated with interstitial cystitis (PBS/IC) is a clinical condition characterized pelvic pain, urinary urgency, and urinary frequency. In this study, 22 patients were assigned to make two visits over a three weeks period. The patients were randomly, double-blinded assigned in two groups. The first group received Cystex® capsules. The second group received placebo capsules. Two capsules were taken three times a day away from meals. The change from baseline in the O'Leary-Sant IC symptom and problem index was the primary outcome parameter. Changes in functional bladder capacity and intensity of pain and urgency have been chosen as secondary outcome parameters. Mood as well as physical and sexual activity were rated by 10 questions on a scale 0 to 6. The ratings were analyzed and the average for each patient in both groups Cystex® and placebo was determined as the quality of life index. For the primary outcome there was a statistically significant difference between the groups. Mean symptom score-sum decreased from 28.4 to 20.5 in the Cystex® group compared with 29.5 to 26.8 in the placebo group (p<0.05). For the secondary end points, pain and urgency intensity improved statistically significantly in the Cystex® group compared with the placebo group (p<0.05). The frequency and functional bladder capacity improved to greater degree in the Cystex® group. The differences were statistically significant for comparison of frequency (p<0.05) and not for functional bladder capacity (p>0.05). In our study, Cystex® enhanced quality of life over the placebo showing a statistically significant. This trial have shown that the efficacy and safety of therapy with Cystex® in the treatment of interstitial cystitis and is an alternative for patients suffering from this pathology. Therefore, it can be concluded that the composition of Cystex®, increased the quality of life in treated patients.
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spelling Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)Clinical trialInterstitial cystitisPainful bladderQuality of lifePainful bladder syndrome associated with interstitial cystitis (PBS/IC) is a clinical condition characterized pelvic pain, urinary urgency, and urinary frequency. In this study, 22 patients were assigned to make two visits over a three weeks period. The patients were randomly, double-blinded assigned in two groups. The first group received Cystex® capsules. The second group received placebo capsules. Two capsules were taken three times a day away from meals. The change from baseline in the O'Leary-Sant IC symptom and problem index was the primary outcome parameter. Changes in functional bladder capacity and intensity of pain and urgency have been chosen as secondary outcome parameters. Mood as well as physical and sexual activity were rated by 10 questions on a scale 0 to 6. The ratings were analyzed and the average for each patient in both groups Cystex® and placebo was determined as the quality of life index. For the primary outcome there was a statistically significant difference between the groups. Mean symptom score-sum decreased from 28.4 to 20.5 in the Cystex® group compared with 29.5 to 26.8 in the placebo group (p<0.05). For the secondary end points, pain and urgency intensity improved statistically significantly in the Cystex® group compared with the placebo group (p<0.05). The frequency and functional bladder capacity improved to greater degree in the Cystex® group. The differences were statistically significant for comparison of frequency (p<0.05) and not for functional bladder capacity (p>0.05). In our study, Cystex® enhanced quality of life over the placebo showing a statistically significant. This trial have shown that the efficacy and safety of therapy with Cystex® in the treatment of interstitial cystitis and is an alternative for patients suffering from this pathology. Therefore, it can be concluded that the composition of Cystex®, increased the quality of life in treated patients.Laboratório de Farmacognosia, Escola de Farmácia Departamento de Farmácia Universidade Federal de Ouro Preto, Minas GeraisFaculdade de Filosofia e Ciências Departamento de Fonoaudiologia Universidade Estadual Paulista, São PauloDepartamento de Farmácia Centro Universitário Fundação Instituto de Ensino para Osasco, OsascoDepartamento de Ciências Biológicas Campus Diadema Universidade Federal de São Paulo, DiademaLaboratório de Pesquisa em Fármacos Universidade Federal do Amapá, Macapá, AmapáDepartamento de Ciências Exatas e da Terra Campus Diadema Universidade Federal de São PauloFaculdade de Filosofia e Ciências Departamento de Fonoaudiologia Universidade Estadual Paulista, São PauloUniversidade Federal de Ouro PretoUniversidade Estadual Paulista (UNESP)Instituto de Ensino para OsascoUniversidade Federal de São Paulo (UNIFESP)Universidade Federal do AmapáSouza, Gustavo H.B.Maistro, Edson L. [UNESP]Rodrigues, MarceloCarvalho, Jose C.T.Fonseca, Fernando L.A.Lopes, Andrey P.Perazzo, Fabio F.2022-04-29T02:43:34Z2022-04-29T02:43:34Z2012-03-07info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article423-427HealthMED, v. 6, n. 2, p. 423-427, 2012.1840-2291http://hdl.handle.net/11449/2267272-s2.0-84857768023Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengHealthMEDinfo:eu-repo/semantics/openAccess2022-04-29T02:43:34Zoai:repositorio.unesp.br:11449/226727Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-29T02:43:34Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)
title Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)
spellingShingle Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)
Souza, Gustavo H.B.
Clinical trial
Interstitial cystitis
Painful bladder
Quality of life
title_short Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)
title_full Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)
title_fullStr Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)
title_full_unstemmed Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)
title_sort Phase II clinical study of an association for the treatment of interstitial cystitis (Cystex®)
author Souza, Gustavo H.B.
author_facet Souza, Gustavo H.B.
Maistro, Edson L. [UNESP]
Rodrigues, Marcelo
Carvalho, Jose C.T.
Fonseca, Fernando L.A.
Lopes, Andrey P.
Perazzo, Fabio F.
author_role author
author2 Maistro, Edson L. [UNESP]
Rodrigues, Marcelo
Carvalho, Jose C.T.
Fonseca, Fernando L.A.
Lopes, Andrey P.
Perazzo, Fabio F.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Ouro Preto
Universidade Estadual Paulista (UNESP)
Instituto de Ensino para Osasco
Universidade Federal de São Paulo (UNIFESP)
Universidade Federal do Amapá
dc.contributor.author.fl_str_mv Souza, Gustavo H.B.
Maistro, Edson L. [UNESP]
Rodrigues, Marcelo
Carvalho, Jose C.T.
Fonseca, Fernando L.A.
Lopes, Andrey P.
Perazzo, Fabio F.
dc.subject.por.fl_str_mv Clinical trial
Interstitial cystitis
Painful bladder
Quality of life
topic Clinical trial
Interstitial cystitis
Painful bladder
Quality of life
description Painful bladder syndrome associated with interstitial cystitis (PBS/IC) is a clinical condition characterized pelvic pain, urinary urgency, and urinary frequency. In this study, 22 patients were assigned to make two visits over a three weeks period. The patients were randomly, double-blinded assigned in two groups. The first group received Cystex® capsules. The second group received placebo capsules. Two capsules were taken three times a day away from meals. The change from baseline in the O'Leary-Sant IC symptom and problem index was the primary outcome parameter. Changes in functional bladder capacity and intensity of pain and urgency have been chosen as secondary outcome parameters. Mood as well as physical and sexual activity were rated by 10 questions on a scale 0 to 6. The ratings were analyzed and the average for each patient in both groups Cystex® and placebo was determined as the quality of life index. For the primary outcome there was a statistically significant difference between the groups. Mean symptom score-sum decreased from 28.4 to 20.5 in the Cystex® group compared with 29.5 to 26.8 in the placebo group (p<0.05). For the secondary end points, pain and urgency intensity improved statistically significantly in the Cystex® group compared with the placebo group (p<0.05). The frequency and functional bladder capacity improved to greater degree in the Cystex® group. The differences were statistically significant for comparison of frequency (p<0.05) and not for functional bladder capacity (p>0.05). In our study, Cystex® enhanced quality of life over the placebo showing a statistically significant. This trial have shown that the efficacy and safety of therapy with Cystex® in the treatment of interstitial cystitis and is an alternative for patients suffering from this pathology. Therefore, it can be concluded that the composition of Cystex®, increased the quality of life in treated patients.
publishDate 2012
dc.date.none.fl_str_mv 2012-03-07
2022-04-29T02:43:34Z
2022-04-29T02:43:34Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv HealthMED, v. 6, n. 2, p. 423-427, 2012.
1840-2291
http://hdl.handle.net/11449/226727
2-s2.0-84857768023
identifier_str_mv HealthMED, v. 6, n. 2, p. 423-427, 2012.
1840-2291
2-s2.0-84857768023
url http://hdl.handle.net/11449/226727
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv HealthMED
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 423-427
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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