2019
DOI: 10.1007/s00228-019-02745-7
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Efficacy of phloroglucinol for the treatment of pain of gynaecologic or obstetrical origin: a systematic review of literature of randomised controlled trials

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Cited by 9 publications
(6 citation statements)
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“…At present, commonly used uterine contraction inhibitors include progesterone, oxytocin antagonist, and PG antagonist (21). Phloroglucinol is a myopathic non-atropine non-papaverine smooth muscle antispasmodic with 1,3,5-trihydroxybenzene as the active ingredient (6), which has no anticholinergic effect, no effect on cardiovascular function, does not cause hypotension, has no teratogenicity, mutagenicity, or carcinogenicity, and no adverse effect on embryo and fetal development (22). In one study, researchers administered 80 mg phloroglucinol intravenously twice a day to IVF-ET-assisted pregnancy patients up to 5 days before embryo transfer, trusting that it could reduce the uterine contraction of patients and increase the clinical pregnancy rate (23).…”
Section: Discussionmentioning
confidence: 99%
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“…At present, commonly used uterine contraction inhibitors include progesterone, oxytocin antagonist, and PG antagonist (21). Phloroglucinol is a myopathic non-atropine non-papaverine smooth muscle antispasmodic with 1,3,5-trihydroxybenzene as the active ingredient (6), which has no anticholinergic effect, no effect on cardiovascular function, does not cause hypotension, has no teratogenicity, mutagenicity, or carcinogenicity, and no adverse effect on embryo and fetal development (22). In one study, researchers administered 80 mg phloroglucinol intravenously twice a day to IVF-ET-assisted pregnancy patients up to 5 days before embryo transfer, trusting that it could reduce the uterine contraction of patients and increase the clinical pregnancy rate (23).…”
Section: Discussionmentioning
confidence: 99%
“…(1) patients aged between 20 and 45 years; (2) patients with a body mass index (BMI) of 18.5-27.9 kg/m 2 ; (3) patients who met the diagnosis of endometriosis (8); (4) patients whose endometrial preparation scheme was a down-regulation scheme of gonadotropin-releasing hormone agonist (GnRH-a); (5) patients with serum cancer antigen 125 (CA 125 ) levels <35 IU/ L on the day of hormone replacement; (6) patients with an endometrial thickness ≥8 mm on progesterone conversion; (7) patients transplanted with 1 high-quality blastocyst or 1-2 cleavage stage embryos, of which at least one was a highquality embryo.…”
Section: Materials and Methods Participantsmentioning
confidence: 99%
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“…Phloroglucinol, a polyphenol trihydroxybenzene with an aromatic phenyl ring and three hydroxyl groups, is a naturally occurring secondary metabolite present in a variety of organisms including plants, algae, and bacteria [ 13 , 14 ]. This phenolic compound is known to have various pharmacological potentials such as antibacterial, anticonvulsant, anti-allergic, antithrombotic, anti-inflammatory, and cancer chemopreventive activities [ 15 , 16 ]. Recently, the antioxidant potential of phloroglucinol has been validated in several in vitro and in vivo models.…”
Section: Introductionmentioning
confidence: 99%
“…Once the ligand–receptor binding occurs, the TMPRSS2 cuts spike glycoprotein and controls the entry of viral envelopes into host cells through various synchronization changes [ 15 ]. The blockade of the ACE receptor can be controlled by inhibiting TMPRSS2 protease inhibition [ 16 , 17 ].…”
Section: Introductionmentioning
confidence: 99%