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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05635422
Other study ID # 2022-01
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 14, 2022
Est. completion date November 14, 2024

Study information

Verified date November 2022
Source Boulogne sur Mer Hospital Center
Contact Guillaume BERTOUX
Phone + 33 3 21 99 87 13
Email g.bertoux@ch-boulogne.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the relevance of carrying out a measure of muscular fatigability by isokinetism, in the search for factors favouring micro-traumatic lesions of the lower limbs in a population of triathletes. This is a prospective monocentric pilot study of the before/after type in which the patient is his or her own control, in high-level triathletes practising an endurance sport, who have had more than 7 consecutive days off running due to a musculoskeletal injury during the previous sporting year.


Recruitment information / eligibility

Status Recruiting
Enrollment 25
Est. completion date November 14, 2024
Est. primary completion date November 14, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Having had a practical running break of more than 7 consecutive days due to a musculoskeletal injury of a lower limb during the previous sport year - Willing to comply with all study procedures - Having given written consent - Socially insured Exclusion Criteria: - Pain that does not allow an isokinetic test to be performed - Knee joint amplitude less than 100° of flexion or flessum greater than 5°. - History of rupture or ligamentoplasty of the anterior cruciate ligament less than 2 years ago - History of knee surgery less than 2 years

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
isokinetism test
measure of muscular fatigability by isokinetism

Locations

Country Name City State
France Boulogne sur mer Hospital Center Boulogne-sur-Mer

Sponsors (1)

Lead Sponsor Collaborator
Boulogne sur Mer Hospital Center

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary fatigue index between the injured leg and the healthy leg To compare the fatigue index between the injured leg and the healthy leg in high level triathletes injured in the previous season. the day of inclusion
Secondary difference of the fatigue index to the difference of the Croisier ratio between the injured leg and the healthy leg Correlate the difference in the fatigue index to the difference in the Croisier ratio between the injured leg and the healthy leg. the day of inclusion
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