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Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCT

Title: Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCT
Authors: Muders, Kerstin; Pilat, Christian; Deuster, Vanessa; Frech, Torsten; Krüger, Karsten; Pons-Kühnemann, Jörn; Mooren, Frank-Christoph
Contributors: Biologische Heilmittel Heel GmbH
Source: Mediators of Inflammation ; volume 2016, page 1-9 ; ISSN 0962-9351 1466-1861
Publisher Information: Wiley
Publication Year: 2016
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: The present double-blind, randomized, placebo-controlled clinical trial intended to test whether ingestion of a natural combination medicine (Tr14 tablets) affects serum muscle damage and inflammatory immune response after downhill running. 96 male subjects received Tr14 tablets, which consist of 14 diluted biological and mineral components, or a placebo for 72 h after the exercise test, respectively. Changes in postexercise levels of various serum muscle damage and immunological markers were investigated. The area under the curve with respect to the increase ( A U C i ) of perceived pain score and creatine kinase (CK) were defined as primary outcome measures. While for CK the p value of the difference between the two groups is borderline, the pain score and muscle strength were not statistically significant. However, a trend towards lower levels of muscle damage (CK, p = 0.05 ; LDH, p = 0.06 ) in the Tr14 group was shown. Less pronounced lymphopenia ( p = 0.02 ), a trend towards a lower expression of CD69 count ( p = 0.07 ), and antigen-stimulated ICAM-1 ( p = 0.01 ) were found in the verum group. The Tr14 group showed a tendentially lower increase of neutrophils ( p = 0.10 ), BDNF ( p = 0.03 ), stem cell factor ( p = 0.09 ), and GM-CSF ( p = 0.09 ) to higher levels. The results of the current study indicate that Tr14 seems to limit exercise-induced muscle damage most likely via attenuation of both innate and adaptive immune responses. This study was registered with ClinicalTrials.gov ( NCT01912469 ).
Document Type: article in journal/newspaper
Language: English
DOI: 10.1155/2016/1693918
Availability: https://doi.org/10.1155/2016/1693918; http://downloads.hindawi.com/journals/mi/2016/1693918.pdf; http://downloads.hindawi.com/journals/mi/2016/1693918.xml
Rights: http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.6EC5F6A9
Database: BASE