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Clinical Trials/NCT00005923
NCT00005923
Unknown
Not Applicable

The Effect of Estrogen and Progesterone Levels on Knee and Ankle Joint Laxity

National Center for Research Resources (NCRR)1 site in 1 countryJune 26, 2000
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
National Center for Research Resources (NCRR)
Locations
1
Last Updated
20 years ago

Overview

Brief Summary

The proposed research is an observational study designed to compare estrogen and progesterone serum levels with knee and ankle joint laxity, and muscle reaction time as a measure of neuromuscular function. Three groups of women athletes with differing estrogen and progesterone profiles (normal menstrual cycles, amenorrheic, and exogenous estrogen supplementation) and one control group (male collegiate athletes) will be used to compare differences in joint laxity and neuromuscular function. Blood levels of estrogen and progesterone will be measured at four time points across the menstrual cycle. Joint laxity and muscle reaction time will also be measured at each of these points. The investigator hypothesizes that knee and ankle joint laxity and muscle reaction time will significantly increase with increasing estrogen and progesterone levels.

Registry
clinicaltrials.gov
Start Date
June 26, 2000
End Date
TBD
Last Updated
20 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
National Center for Research Resources (NCRR)

Eligibility Criteria

Inclusion Criteria

  • pre-collegiate or collegiate athletes

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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