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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT05722301
Other study ID # 2
Secondary ID
Status Withdrawn
Phase Phase 3
First received
Last updated
Start date November 1, 2019
Est. completion date November 1, 2021

Study information

Verified date February 2023
Source American Hip Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized-controlled trial will study on the effect of testosterone therapy on patients undergoing total hip replacement. Subjects will be male patients > 50 years with testosterone deficiency undergoing total hip replacement due to severe degenerative joint disease. All participants will receive a total hip replacement and will be randomized to either testosterone therapy or placebo. A total of 80 subjects will be recruited randomized into 2 groups of 40 subjects. Testosterone therapy will be administered once to each patient at 2 weeks before surgery. The long-term follow up will be the same as all patients with patient-reported outcomes after total hip replacement, VAS for pain and satisfaction at regular intervals.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date November 1, 2021
Est. primary completion date November 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 50 Years and older
Eligibility Inclusion Criteria: - Male patients - 50 years of age and older - Individuals who have degenerative joint disease requiring total hip replacement after failure of conservative measures. Exclusion Criteria: - History of prostate cancer less than 5 years ago or those men whom are not considered to be cancer free - History of breast cancer less than 5 years ago or those men whom are not considered to be cancer free - History of deep vein thrombosis (DVT) - Presence of Factor V Leiden (as seen in labs) - Presence of Protein S Deficiency (as seen in labs) - History of atherosclerotic artery disease - by history having had a diagnosis made of CAD, MI, or stroke - Liver disease (as viewed by liver function tests) - Testosterone free level greater than 10pg/mL - Hematocrit >51%; PSA >= 3ng/mL.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Testosterone Therapy
The testosterone pellet implantation will be performed 2 weeks before surgery. The dose is determined by baseline levels of sex hormone binding globulin (SHBG) in the following manner: If SHBG > 60nmol/L implant 5 Testosterone Compounded 200mg (total 1000mgs testosterone). If SHBG 41-59 nmol/L implant 4 Testosterone Compounded 200mg (total 800mgs testosterone). If SHBG <40 nmol/L implant 3 Testosterone Compounded 200mg (total 600mgs testosterone).
Other:
No Testosterone Therapy
For the sham procedure no pellets will be implanted.

Locations

Country Name City State
United States American Hip Institute Research Foundation Des Plaines Illinois

Sponsors (1)

Lead Sponsor Collaborator
American Hip Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Harris Hip Score patient-reported outcome measure 3 months
Primary Harris Hip Score patient-reported outcome measure 1 year
Primary Forgotten Joint Score patient-reported outcome measure 3 months
Primary Forgotten Joint Score patient-reported outcome measure 1 year
Secondary Visual Analog Scale patient-reported outcome measure 3 months
Secondary Visual Analog Scale patient-reported outcome measure 1 year
Secondary Patient Satisfaction (reported from questionnaire) patient-reported outcome measure 3 months
Secondary Patient Satisfaction (reported from questionnaire) patient-reported outcome measure 1 year
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