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serrapeptase-pain

A Randomized, Double-blind, Placebo-controlled Study Comparing The Efficacy And Safety Of Paracetamol, Serratiopeptidase, Ibuprofen And Betamethasone Using The Dental Impaction Pain Model

効果 なし
試験方法 二重盲検法
試験期間 1-7 日
被験者数 150
性別 男女
年齢 18-29, 30-44, 45-64
体型 肥満, 平均
この研究の注釈:

Relative to the comparator drugs (betamethasone and paracetamol), serrapeptase was less effective in reducing pain and inflammation associated with third molar surgery when taken at the standard 30mg dosage; relative to placebo, there was no significant difference.


Comparison Of The Roles Of Serratiopeptidase And Dexamethasone In The Control Of Inflammation And Trismus Following Impacted Third Molar Surgery
効果 減少
試験方法 二重盲検法
試験期間 1-7 日
被験者数 110
性別 男女
年齢 18-29, 30-44, 45-64, 65+
体型 肥満, 平均
この研究の注釈:

In patients undergoing jaw surgery (removal of third molar), 30mg serrapeptase daily for up to a week was more effective than placebo in reducing pain and swelling although trismus (opening of the jaw) was unaffected.


The Treatment Of Breast Engorgement With Serrapeptase (Danzen): A Randomised Double-blind Controlled Trial
効果 減少
試験方法 二重盲検法
試験期間 1-7 日
被験者数 70
性別 女性
年齢 18-29, 30-44
体型 平均
この研究の注釈:

10mg serrapeptase thrice daily (30mg total) for 3 days in women with breast engorgement was able to reduce pain and tenderness as assessed by self-report surveys.


Clinical Study Of The Efficacy Of And Tolerance To Seaprose S In Inflammatory Venous Disease. Controlled Study Versus Serratio-peptidase
効果 減少
試験方法 コホート法
試験期間 1-2 週間
被験者数 40
性別 男女
年齢 30-44, 45-64, 65+
体型 平均
この研究の注釈:

In persons with superficial thrombophlebitis given 30mg serrapeptase (10mg thrice daily) relative to the comparator drug Protease S (Seaprose S; no placebo control in this study) noted that both drugs were able to reduce pain and symptoms of thrombophlebitis, but the symptoms alleviation seen with serrapeptase (65%) was outperformed by protease S (85%).


Evaluation Of Serratia Peptidase In Acute Or Chronic Inflammation Of Otorhinolaryngology Pathology: A Multicentre, Double-blind, Randomized Trial Versus Placebo
効果 減少
試験方法 二重盲検法
試験期間 1-2 週間
被験者数 193
性別 男女
年齢 18-29, 30-44, 45-64, 65+
この研究の注釈:

In persons with acute or chronic ear, nose or throat disorders given 10mg of serrapeptase thrice daily (30mg total), supplementation was more effective than placebo in reducing abnormalities of mucus production and swallowing and was also analgesic.


管理人 :慶應義塾大学の理工学部卒業後、国内外でコンサルティング業務やスタートアップの立ち上げを経験した後、日本に帰国してから健康・医療の情報を収集して発信しています。 趣味:ネットサーフィン、読書(最近かなり減ってますが)、アウトドア(家族と) 毎日メディテーションとジョギング、筋トレ・ストレッチしています。既婚で子供4人(男女女男)です。