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

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...

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Main Authors: Kerstin Muders, Christian Pilat, Vanessa Deuster, Torsten Frech, Karsten Krüger, Jörn Pons-Kühnemann, Frank-Christoph Mooren
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2016/1693918
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spelling doaj-2b3088ab571a4cd4a61a440a6f03b6d02020-11-24T21:32:42ZengHindawi LimitedMediators of Inflammation0962-93511466-18612016-01-01201610.1155/2016/16939181693918Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCTKerstin Muders0Christian Pilat1Vanessa Deuster2Torsten Frech3Karsten Krüger4Jörn Pons-Kühnemann5Frank-Christoph Mooren6Department of Sports Medicine, Justus Liebig University, Kugelberg 62, 35394 Giessen, GermanyDepartment of Sports Medicine, Justus Liebig University, Kugelberg 62, 35394 Giessen, GermanyDepartment of Sports Medicine, Justus Liebig University, Kugelberg 62, 35394 Giessen, GermanyDepartment of Sports Medicine, Justus Liebig University, Kugelberg 62, 35394 Giessen, GermanyDepartment of Sports Medicine, Justus Liebig University, Kugelberg 62, 35394 Giessen, GermanyMedical Statistics, Justus Liebig University, Heinrich-Buff-Ring 44, 35392 Giessen, GermanyDepartment of Sports Medicine, Justus Liebig University, Kugelberg 62, 35394 Giessen, GermanyThe 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 (AUCi) 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).http://dx.doi.org/10.1155/2016/1693918
collection DOAJ
language English
format Article
sources DOAJ
author Kerstin Muders
Christian Pilat
Vanessa Deuster
Torsten Frech
Karsten Krüger
Jörn Pons-Kühnemann
Frank-Christoph Mooren
spellingShingle Kerstin Muders
Christian Pilat
Vanessa Deuster
Torsten Frech
Karsten Krüger
Jörn Pons-Kühnemann
Frank-Christoph Mooren
Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCT
Mediators of Inflammation
author_facet Kerstin Muders
Christian Pilat
Vanessa Deuster
Torsten Frech
Karsten Krüger
Jörn Pons-Kühnemann
Frank-Christoph Mooren
author_sort Kerstin Muders
title Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCT
title_short Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCT
title_full Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCT
title_fullStr Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCT
title_full_unstemmed Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCT
title_sort effects of traumeel (tr14) on exercise-induced muscle damage response in healthy subjects: a double-blind rct
publisher Hindawi Limited
series Mediators of Inflammation
issn 0962-9351
1466-1861
publishDate 2016-01-01
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 (AUCi) 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).
url http://dx.doi.org/10.1155/2016/1693918
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