Cargando…

Investigating the effect of vitamin D vaginal suppository on sexual function among postmenopausal women: study protocol for a randomized controlled trial

BACKGROUND: Menopause is associated with changes in sexual function which are partly due to vaginal atrophy in response to estrogen reduction. Estrogen administration temporarily reduces the symptoms of vaginal dryness, but long-term exposure to this drug is likely to be associated with serious comp...

Descripción completa

Detalles Bibliográficos
Autores principales: Sarebani, Zinat, Alimoradi, Zainab, Aali, Ehsan, Mirzadeh, Monirsadat, Chegini, Venus, Abbaspour, Mohammadreza, Griffiths, Mark D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029522/
https://www.ncbi.nlm.nih.gov/pubmed/32070323
http://dx.doi.org/10.1186/s12905-020-00899-6
_version_ 1783499186190155776
author Sarebani, Zinat
Alimoradi, Zainab
Aali, Ehsan
Mirzadeh, Monirsadat
Chegini, Venus
Abbaspour, Mohammadreza
Griffiths, Mark D.
author_facet Sarebani, Zinat
Alimoradi, Zainab
Aali, Ehsan
Mirzadeh, Monirsadat
Chegini, Venus
Abbaspour, Mohammadreza
Griffiths, Mark D.
author_sort Sarebani, Zinat
collection PubMed
description BACKGROUND: Menopause is associated with changes in sexual function which are partly due to vaginal atrophy in response to estrogen reduction. Estrogen administration temporarily reduces the symptoms of vaginal dryness, but long-term exposure to this drug is likely to be associated with serious complications. Considering the promising results of previous studies concerning the effect of vitamin D on vaginal dryness, the proposed study will investigate the effect of vitamin D vaginal suppository on the sexual function of postmenopausal women. METHODS: In a randomized, controlled clinical trial, 105 postmenopausal women will be randomly assigned to three groups receiving vitamin D vaginal suppository, placebo vaginal suppository, or control (no intervention). Vitamin D vaginal suppositories contain 1000 units of vitamin D3. The timing of the use of vitamin D vaginal suppositories and placebo suppositories will be every night in the first 2 weeks, and every other night in the following 6 weeks (8 weeks in total). The primary outcome will be the sexual function of participants which will be assessed using the Female Sexual Function Index (FSFI) before and immediately after the intervention, and at 1 and 2 months after the end of the intervention. The side effects of these suppositories will be examined as a secondary consequence of the study. Data will be analyzed using SPSS software version 25. In the case of normal distribution of data, the mean score of sexual function will be compared between the groups using a repeated measurements ANOVA. If statistical analysis leads to significant results, the post-hoc test will be used to determine the differences between the groups. Comparison of demographic and fertility characteristics of the women will be carried out using statistical tests such as chi-squares and t-tests. A significance level of p < .05 will be used for statistical analyses. DISCUSSION: If vitamin D vaginal suppositories improve sexual function among premenopausal women with long-term effects and minimum side effects, the suppositories will be considered a safe complementary and alternative choice for alleviating sexual dysfunction among this group. TRIAL REGISTRATION: IRCT20180704040346N1 at 2018-10-13 prospectively registered.
format Online
Article
Text
id pubmed-7029522
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-70295222020-02-25 Investigating the effect of vitamin D vaginal suppository on sexual function among postmenopausal women: study protocol for a randomized controlled trial Sarebani, Zinat Alimoradi, Zainab Aali, Ehsan Mirzadeh, Monirsadat Chegini, Venus Abbaspour, Mohammadreza Griffiths, Mark D. BMC Womens Health Study Protocol BACKGROUND: Menopause is associated with changes in sexual function which are partly due to vaginal atrophy in response to estrogen reduction. Estrogen administration temporarily reduces the symptoms of vaginal dryness, but long-term exposure to this drug is likely to be associated with serious complications. Considering the promising results of previous studies concerning the effect of vitamin D on vaginal dryness, the proposed study will investigate the effect of vitamin D vaginal suppository on the sexual function of postmenopausal women. METHODS: In a randomized, controlled clinical trial, 105 postmenopausal women will be randomly assigned to three groups receiving vitamin D vaginal suppository, placebo vaginal suppository, or control (no intervention). Vitamin D vaginal suppositories contain 1000 units of vitamin D3. The timing of the use of vitamin D vaginal suppositories and placebo suppositories will be every night in the first 2 weeks, and every other night in the following 6 weeks (8 weeks in total). The primary outcome will be the sexual function of participants which will be assessed using the Female Sexual Function Index (FSFI) before and immediately after the intervention, and at 1 and 2 months after the end of the intervention. The side effects of these suppositories will be examined as a secondary consequence of the study. Data will be analyzed using SPSS software version 25. In the case of normal distribution of data, the mean score of sexual function will be compared between the groups using a repeated measurements ANOVA. If statistical analysis leads to significant results, the post-hoc test will be used to determine the differences between the groups. Comparison of demographic and fertility characteristics of the women will be carried out using statistical tests such as chi-squares and t-tests. A significance level of p < .05 will be used for statistical analyses. DISCUSSION: If vitamin D vaginal suppositories improve sexual function among premenopausal women with long-term effects and minimum side effects, the suppositories will be considered a safe complementary and alternative choice for alleviating sexual dysfunction among this group. TRIAL REGISTRATION: IRCT20180704040346N1 at 2018-10-13 prospectively registered. BioMed Central 2020-02-18 /pmc/articles/PMC7029522/ /pubmed/32070323 http://dx.doi.org/10.1186/s12905-020-00899-6 Text en © The Author(s) 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Sarebani, Zinat
Alimoradi, Zainab
Aali, Ehsan
Mirzadeh, Monirsadat
Chegini, Venus
Abbaspour, Mohammadreza
Griffiths, Mark D.
Investigating the effect of vitamin D vaginal suppository on sexual function among postmenopausal women: study protocol for a randomized controlled trial
title Investigating the effect of vitamin D vaginal suppository on sexual function among postmenopausal women: study protocol for a randomized controlled trial
title_full Investigating the effect of vitamin D vaginal suppository on sexual function among postmenopausal women: study protocol for a randomized controlled trial
title_fullStr Investigating the effect of vitamin D vaginal suppository on sexual function among postmenopausal women: study protocol for a randomized controlled trial
title_full_unstemmed Investigating the effect of vitamin D vaginal suppository on sexual function among postmenopausal women: study protocol for a randomized controlled trial
title_short Investigating the effect of vitamin D vaginal suppository on sexual function among postmenopausal women: study protocol for a randomized controlled trial
title_sort investigating the effect of vitamin d vaginal suppository on sexual function among postmenopausal women: study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029522/
https://www.ncbi.nlm.nih.gov/pubmed/32070323
http://dx.doi.org/10.1186/s12905-020-00899-6
work_keys_str_mv AT sarebanizinat investigatingtheeffectofvitamindvaginalsuppositoryonsexualfunctionamongpostmenopausalwomenstudyprotocolforarandomizedcontrolledtrial
AT alimoradizainab investigatingtheeffectofvitamindvaginalsuppositoryonsexualfunctionamongpostmenopausalwomenstudyprotocolforarandomizedcontrolledtrial
AT aaliehsan investigatingtheeffectofvitamindvaginalsuppositoryonsexualfunctionamongpostmenopausalwomenstudyprotocolforarandomizedcontrolledtrial
AT mirzadehmonirsadat investigatingtheeffectofvitamindvaginalsuppositoryonsexualfunctionamongpostmenopausalwomenstudyprotocolforarandomizedcontrolledtrial
AT cheginivenus investigatingtheeffectofvitamindvaginalsuppositoryonsexualfunctionamongpostmenopausalwomenstudyprotocolforarandomizedcontrolledtrial
AT abbaspourmohammadreza investigatingtheeffectofvitamindvaginalsuppositoryonsexualfunctionamongpostmenopausalwomenstudyprotocolforarandomizedcontrolledtrial
AT griffithsmarkd investigatingtheeffectofvitamindvaginalsuppositoryonsexualfunctionamongpostmenopausalwomenstudyprotocolforarandomizedcontrolledtrial