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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03933618
Other study ID # 4134
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date April 2, 2015
Est. completion date March 8, 2017

Study information

Verified date October 2019
Source Albany Medical College
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates anastrazole and clomiphene in the improvement in hypogonadal symptoms and erectile function. Each subject will receive Anastrazole 1 mg/day, clomiphene 25 mg/day and placebo in randomized schedule of 8 week intervals.


Description:

Aromatase inhibitors (AI) (Anastrazole) and selective estrogen receptor modifiers (SERMS)(clomiphene) increase testosterone production through stimulation of the hypothalamic pituitary axis. While these drugs both reduce the feedback inhibition of estrogen on the pituitary, SERMs cause an increase in serum estradiol, whereas AIs reduce estradiol levels. Using these medications, we can obtain therapeutic testosterone levels with either an increase or decrease in estradiol levels.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date March 8, 2017
Est. primary completion date March 8, 2017
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

1. Men age 18-70

2. Baseline morning Testosterone 150-350 ng/dL x2

3. leutenizing hormone (LH) 1.5-9.2 miU/mL, Follicle stimulation hormone (FSH) 1.6-8.0 miU/mL, Prolactin 4-15 ng/mL

4. Positive Androgen Deficiency in the Aging Male (ADAM) score. A positive score is when an affirmative answer (''yes'') to either questions "Do you have a decreased sex drive/libido?" or "Are your erections less strong?" or any three other questions.10

5. Body mass index (BMI) <40

6. Sexual health inventory for men (SHIM) score >7 and <21. Patients are allowed to be taking phosphodiesterase 5 inhibitors (i.e. Viagra, Levitra, Cialis) at baseline, however we will ask them to do the SHIM survey as if they were not taking this medication.

7. Men must attempt to have at least four sexual encounters over each of the eight-week periods

8. Men willing not to take phosphodiesterase 5 inhibitors throughout the entire study

Exclusion Criteria:

1. Current or previous history of prostate cancer

2. Previous or current androgen deprivation therapy for prostate cancer,

3. Past surgical history of prostatectomy.

4. History of testicular cancer.

5. History of deep vein thrombosis (DVT) or blood dyscrasia

6. History of breast cancer

7. Men with past or current treatment for erectile dysfunction including MUSE (alprostodil), intracavernosal injections, penile prosthesis. Men not on treatment or men who are on phosphodiesterase inhibitors will be allowed to be in the study but must stop their use at the screening visit.

8. Chronic opioid use

9. Use of steroids within the past 3 months, including prednisone and/or cortisone injections, and inhaled steroids. Topical steroid cream is acceptable.

10. History of or current use of anabolic steroids, i.e. testosterone, (or any analog of testosterone) dihydroepiandrosterone (DHEA), dihydroepiandrosterone sulfate (DHEAS) or any growth promoters i.e. growth hormone itself or analogs of growth hormone

11. History of or current use of anti-androgen medications, i.e. Aldactone, Tagamet, estrogens

12. Alcohol intake > 30 grams (drink more than 2 beers per day OR more than 1 glass of wine or cocktail daily)

13. Having started a new medication during the past three months which may interfere with the outcome measures of the study

14. Polycythemia (HCT >52% )

15. History of prostate specific antigen (PSA)> 4.0 ng/dl

16. Hematocrit (HCT)< 36 %

17. Liver function tests greater than 2 times upper normal limits or history of abnormal electrolytes, calcium or Parathyroid hormone without workup, at the discretion of the investigator.

18. Previous hypogonadal treatment within last 3 months. -

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Anastrozole 1mg

Clomiphene Citrate 25mg

Placebo - Cap


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Albany Medical College Laboratory Corporation of America

Outcome

Type Measure Description Time frame Safety issue
Primary IIEF (International Index of Erectile Function) Score - Screen 15 item self reported erectile function. Each item is scored 0-5 with 0=negative response and 5 = positive response with totals of 0-75 At baseline
Primary IIEF (International Index of Erectile Function) Score - Week 8 15 item self reported erectile function over the past 8 weeks. Each item is scored 0-5 with 0=negative response and 5 = positive response with totals of 0-75 Week 8
Primary IIEF (International Index of Erectile Function) Score - Week 16 15 item self reported erectile function over the past 8 weeks. Each item is scored 0-5 with 0=negative response and 5 = positive response with totals of 0-75 Week 16
Primary IIEF (International Index of Erectile Function) Score - Week 24 15 item self reported erectile function over the past 8 weeks. Each item is scored 0-5 with 0=negative response and 5 = positive response with totals of 0-75 Week 24
Secondary Normalized Testosterone - Screen Normalized at >350ng/dl Baseline
Secondary Normalized Testosterone - Week 8 Normalized at >350ng/dl Week 8
Secondary Normalized Testosterone - Week 16 Normalized at >350ng/dl Week 16
Secondary Normalized Testosterone - Week 24 Normalized at >350ng/dl Week 24
Secondary ADAM (Androgen Deficiency in the Aging Male) Score - Screen Self reported quantification of hypogonadism. 10 "yes" or "no" questions.
A positive (yes) questionnaire result is defined as a "yes or 1" and a negative (no) questionnaire result is defined as a "no or 0" to question 1 or question 7 or any 3 other questions.
Yes (1) represents a better outcome than No (1)
In Data Entry:
Yes - 1 No - 0
Baseline
Secondary ADAM (Androgen Deficiency in the Aging Male) Score - Week 8 Self reported quantification of hypogonadism. 10 "yes" or "no" questions.
A positive (yes) questionnaire result is defined as a "yes or 1" and a negative (no) questionnaire result is defined as a "no or 0" to question 1 or question 7 or any 3 other questions.
Yes (1) represents a better outcome than No (1)
In Data Entry:
Yes - 1 No - 0
Week 8
Secondary ADAM (Androgen Deficiency in the Aging Male) Score - Week 16 Self reported quantification of hypogonadism. 10 "yes" or "no" questions.
A positive (yes) questionnaire result is defined as a "yes or 1" and a negative (no) questionnaire result is defined as a "no or 0" to question 1 or question 7 or any 3 other questions.
Yes (1) represents a better outcome than No (1)
In Data Entry:
Yes - 1 No - 0
Week 16
Secondary ADAM (Androgen Deficiency in the Aging Male) Score - Week 24 Self reported quantification of hypogonadism. 10 "yes" or "no" questions.
A positive (yes) questionnaire result is defined as a "yes or 1" and a negative (no) questionnaire result is defined as a "no or 0" to question 1 or question 7 or any 3 other questions.
Yes (1) represents a better outcome than No (1)
In Data Entry:
Yes - 1 No - 0
Week 24
Secondary EHS (Erectile Hardness Score) - Screen Self reported questionnaire rated 0-4 0=penis does not enlarge, 4=Penis completely hard and fully rigid Baseline
Secondary EHS (Erectile Hardness Score) - Week 8 Self reported questionnaire rated 0-4 0=penis does not enlarge, 4=Penis completely hard and fully rigid Week 8
Secondary EHS (Erectile Hardness Score) - Week 16 Self reported questionnaire rated 0-4 0=penis does not enlarge, 4=Penis completely hard and fully rigid Week 16
Secondary EHS (Erectile Hardness Score) - Week 24 Self reported questionnaire rated 0-4 0=penis does not enlarge, 4=Penis completely hard and fully rigid Week 24
Secondary LH - Screen Luteinizing Hormone levels collected at the initial encounter and at the end of the 8, 16, and 24 week periods. Baseline
Secondary LH - Week 8 Luteinizing Hormone levels collected at the initial encounter and at the end of the 8, 16, and 24 week periods. Week 8
Secondary LH - Week 16 Luteinizing Hormone levels collected at the initial encounter and at the end of the 8, 16, and 24 week periods. Week 16
Secondary LH - Week 24 Luteinizing Hormone levels collected at the initial encounter and at the end of the 8, 16, and 24 week periods. Week 24
Secondary FSH - Screen Lab Values for follicle stimulating hormone Baseline
Secondary FSH - Week 8 Lab Values for follicle stimulating hormone Week 8
Secondary FSH - Week 16 Lab Values for follicle stimulating hormone Week 16
Secondary FSH - Week 24 Lab Values for follicle stimulating hormone Week 24
Secondary Free Testosterone - Screen Measure of Free Testosterone Baseline
Secondary Free Testosterone - Week 8 Measure of Free Testosterone Week 8
Secondary Free Testosterone - Week 16 Measure of Free Testosterone Week 16
Secondary Free Testosterone - Week 24 Measure of Free Testosterone Week 24
Secondary Estradiol - Screen Measurement of Estradiol levels at initial encounter and at the end of Weeks 8, 16, and 24 Baseline
Secondary Estradiol - Week 8 Measurement of Estradiol levels at initial encounter and at the end of Weeks 8, 16, and 24 An entered value of 4.9 means the measure was <5 Week 8
Secondary Estradiol - Week 16 Measurement of Estradiol levels at initial encounter and at the end of Weeks 8, 16, and 24 An entered value of 4.9 means the measure was <5 Week 16
Secondary Estradiol - Week 24 Measurement of Estradiol levels at initial encounter and at the end of Weeks 8, 16, and 24 An entered value of 4.9 means the measure was <5 Week 24
Secondary SHBG - Screen Lab Measure of sex hormone binding globulin at the initial encounter and at the ends of week 8, 16, and 24 Baseline
Secondary SHBG - Week 8 Lab Measure of sex hormone binding globulin at the initial encounter and at the ends of week 8, 16, and 24 Week 8
Secondary SHBG - Week 16 Lab Measure of sex hormone binding globulin at the initial encounter and at the ends of week 8, 16, and 24 Week 16
Secondary SHBG - Week 24 Lab Measure of sex hormone binding globulin at the initial encounter and at the ends of week 8, 16, and 24 Week 24
Secondary SEP #1-3 Cumulative - Screen Questions 1, 2, and 3 for the Sexual Encounter Profile have been cumulatively added. 1 - yes and 0 - no have been added for questions 1-3 to determine a total value from 0-3.
0-3: cumulative score from SEP questions 1, 2, and 3
Higher values (3) are considered to be a better outcomes relative to lower numbers (0) 3 is better than 2 is better than 1 is better than 0
Baseline
Secondary SEP #1-3 Cumulative - Week 8 Questions 1, 2, and 3 for the Sexual Encounter Profile have been cumulatively added. 1 - yes and 0 - no have been added for questions 1-3 to determine a total value from 0-3.
0-3: cumulative score from SEP questions 1, 2, and 3
Higher values (3) are considered to be a better outcomes relative to lower numbers (0) 3 is better than 2 is better than 1 is better than 0
Week 8
Secondary SEP #1-3 Cumulative - Week 16 Questions 1, 2, and 3 for the Sexual Encounter Profile have been cumulatively added. 1 - yes and 0 - no have been added for questions 1-3 to determine a total value from 0-3.
0-3: cumulative score from SEP questions 1, 2, and 3
Higher values (3) are considered to be a better outcomes relative to lower numbers (0) 3 is better than 2 is better than 1 is better than 0
Week 16
Secondary SEP #1-3 Cumulative - Week 24 Questions 1, 2, and 3 for the Sexual Encounter Profile have been cumulatively added. 1 - yes and 0 - no have been added for questions 1-3 to determine a total value from 0-3.
0-3: cumulative score from SEP questions 1, 2, and 3
Higher values (3) are considered to be a better outcomes relative to lower numbers (0) 3 is better than 2 is better than 1 is better than 0
Week 24
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