To evaluate the efficacy and safety of PLC in perimenopausal or postmenopausal women with Hot Flashes: study protocol for a randomized controlled trial

Abstract Background Hot flashes are the most frequent symptoms of the menopause, with 10–20% of all postmenopausal women reporting nearly intolerable occurrences. Although pharmacopuncture with hominis placenta extract is one of the new acupuncture therapies popular in East Asian medicine with a kno...

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Main Authors: Su-Ji Choi, Dong-Il Kim
Format: Article
Language:English
Published: BMC 2019-07-01
Series:Trials
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13063-019-3482-5
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author Su-Ji Choi
Dong-Il Kim
author_facet Su-Ji Choi
Dong-Il Kim
author_sort Su-Ji Choi
collection DOAJ
description Abstract Background Hot flashes are the most frequent symptoms of the menopause, with 10–20% of all postmenopausal women reporting nearly intolerable occurrences. Although pharmacopuncture with hominis placenta extract is one of the new acupuncture therapies popular in East Asian medicine with a known efficacy in treating facial flushing, there has been little research on the efficacy and safety of this extract. This study, therefore, aims to evaluate the efficacy and safety of pharmacopuncture with hominis placenta extract (PLC) compared to injections of normal saline, in perimenopausal and postmenopausal women in Korea. Methods/design This study is a randomized placebo-controlled single-blind multi-center parallel-design trial. In total, 128 perimenopausal or postmenopausal women who meet the inclusion criteria will be recruited. The treatment group will receive PLC pharmacopuncture twice a week, for a total of 18 sessions over 9 weeks. The control group will receive injections of normal saline at the same acupoints during the same period. The post-treatment follow-up assessment will occur 4 weeks after the participant has completed the treatment. Discussion We believe that this trial will provide evidence for the efficacy and safety of PLC pharmacopuncture as a treatment for hot flashes in perimenopausal and postmenopausal women. Trial registration Clinical Research Information Service (CRIS), Republic of Korea, ID: KCT0003533, Registered on 20 February 2019.
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spelling doaj.art-fb7e3ae0a9164b8c80a44eb392dd6d032022-12-21T20:50:24ZengBMCTrials1745-62152019-07-012011810.1186/s13063-019-3482-5To evaluate the efficacy and safety of PLC in perimenopausal or postmenopausal women with Hot Flashes: study protocol for a randomized controlled trialSu-Ji Choi0Dong-Il Kim1Department of Obstetrics & Gynecology, College of Korean Medicine, Dongguk University Korean Medicine HospitalDepartment of Obstetrics & Gynecology, College of Korean Medicine, Dongguk University Korean Medicine HospitalAbstract Background Hot flashes are the most frequent symptoms of the menopause, with 10–20% of all postmenopausal women reporting nearly intolerable occurrences. Although pharmacopuncture with hominis placenta extract is one of the new acupuncture therapies popular in East Asian medicine with a known efficacy in treating facial flushing, there has been little research on the efficacy and safety of this extract. This study, therefore, aims to evaluate the efficacy and safety of pharmacopuncture with hominis placenta extract (PLC) compared to injections of normal saline, in perimenopausal and postmenopausal women in Korea. Methods/design This study is a randomized placebo-controlled single-blind multi-center parallel-design trial. In total, 128 perimenopausal or postmenopausal women who meet the inclusion criteria will be recruited. The treatment group will receive PLC pharmacopuncture twice a week, for a total of 18 sessions over 9 weeks. The control group will receive injections of normal saline at the same acupoints during the same period. The post-treatment follow-up assessment will occur 4 weeks after the participant has completed the treatment. Discussion We believe that this trial will provide evidence for the efficacy and safety of PLC pharmacopuncture as a treatment for hot flashes in perimenopausal and postmenopausal women. Trial registration Clinical Research Information Service (CRIS), Republic of Korea, ID: KCT0003533, Registered on 20 February 2019.http://link.springer.com/article/10.1186/s13063-019-3482-5MenopausePostmenopausal syndromeHot flashesPharmacoacupunctureHominis placentaPharmacopuncture
spellingShingle Su-Ji Choi
Dong-Il Kim
To evaluate the efficacy and safety of PLC in perimenopausal or postmenopausal women with Hot Flashes: study protocol for a randomized controlled trial
Trials
Menopause
Postmenopausal syndrome
Hot flashes
Pharmacoacupuncture
Hominis placenta
Pharmacopuncture
title To evaluate the efficacy and safety of PLC in perimenopausal or postmenopausal women with Hot Flashes: study protocol for a randomized controlled trial
title_full To evaluate the efficacy and safety of PLC in perimenopausal or postmenopausal women with Hot Flashes: study protocol for a randomized controlled trial
title_fullStr To evaluate the efficacy and safety of PLC in perimenopausal or postmenopausal women with Hot Flashes: study protocol for a randomized controlled trial
title_full_unstemmed To evaluate the efficacy and safety of PLC in perimenopausal or postmenopausal women with Hot Flashes: study protocol for a randomized controlled trial
title_short To evaluate the efficacy and safety of PLC in perimenopausal or postmenopausal women with Hot Flashes: study protocol for a randomized controlled trial
title_sort to evaluate the efficacy and safety of plc in perimenopausal or postmenopausal women with hot flashes study protocol for a randomized controlled trial
topic Menopause
Postmenopausal syndrome
Hot flashes
Pharmacoacupuncture
Hominis placenta
Pharmacopuncture
url http://link.springer.com/article/10.1186/s13063-019-3482-5
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