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Effects of Traumeel®S Tablets on Exercise Induced Muscle Damage and Muscle Soreness

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01912469
Enrollment
96
Registered
2013-07-31
Start date
2010-04-30
Completion date
2013-08-31
Last updated
2013-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise-induced Muscle Soreness

Keywords

Muscle, exercise, soreness, Damage, Traumeel

Brief summary

To investigate and compare the effects of Traumeel®S tablets versus placebo on exercise induced muscle damage and muscle soreness for 72 hours after strenuous eccentric exercise test on downhill treadmill.

Interventions

oral, Day 1: one tablet every 15 minutes for two hours after the exercise test, 6 hours and 10 hours after the exercise test; Day 2 and 3: two tablets thrice daily; Day 4: two tablets in the morning

DRUGPlacebo

oral, Day 1: one tablet every 15 minutes for two hours after the exercise test, 6 hours and 10 hours after the exercise test; Day 2 and 3: two tablets thrice daily; Day 4: two tablets in the morning

Sponsors

Biologische Heilmittel Heel GmbH
CollaboratorINDUSTRY
University of Giessen
CollaboratorOTHER
Prof. Dr. med. Frank Christoph Mooren
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Sex: male * Age ≥ 18 and ≤ 40 years * BMI ≥ 18.5 and \< 27,5 kg/m2 (WHO standard for normal range BMI) \[48\] * Maximum relative oxygen uptake (VO2max) \< 53 ml/kg x min * General state of good health * Non-smoker * Medically approved unrestricted participation in sports as shown by diagnostic performance test conducted on treadmill no longer than 3 months prior to study entry * Willingness to provide signed informed consent

Exclusion criteria

* Regular eccentric exercise training * Weekly training volume ≥ 6 hours * Use of dietary supplements (incl. high-dosed vitamins and minerals) * Chronic immune deficiency * Current infection * Heart and/or circulation disorders * Abnormal findings on exercise ECG * Musculoskeletal disorders * Any current clinical condition that requires systemic treatment or might have an impact on study objectives * Hypersensitivity to botanicals of the Compositae family (e.g. Echinacea) * Lactose intolerance * Illicit drug or alcohol abuse * Participation in another clinical trial within 4 weeks prior to study entry

Design outcomes

Primary

MeasureTime frame
Changes in post-exercise two baseline levels up to 72-hours of primary muscle damage marker creatine kinase (CK)72 hours
Changes in post-exercise two baseline levels up to 72-hours Short Form McGill Questionnaire total scores and separate VAS pain ratings72 hours

Secondary

MeasureTime frame
Changes in post-exercise two baseline levels up to 72-hours of immunomodulators (35 lab parameters)72 hours
Changes in post-exercise two baseline levels up to 72-hours of immune status and activation markers (7 lab parameters)72 hours
Changes in post-exercise two baseline levels up to 72-hours of maximum isometric strength (thigh flexors and extensors)72 hours
Changes in post-exercise two baseline levels up to 72-hours of muscle marker Lactate Dehydrogenase72 hours

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026