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Effect of testosterone on androgen deficiency

Evaluation of therapeutic effect of long acting testosterone ampule in Patients with androgen deficiency syndrome presented at urology clinics of Ahwaz.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104236258N1
Enrollment
24
Registered
2011-05-22
Start date
2010-05-25
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Androgen deficiency syndrome. Testicular hypogonadism NOS

Interventions

Intervention 1: Control group: three intramusculare injection of Enanthate testosterone 250MG with three-week intervals. Intervention 2: Intervention group: four intramuscular injection of Enantha
Treatment - Drugs
Control group: three intramusculare injection of Enanthate testosterone 250MG with three-week intervals
Intervention group: four intramuscular injection of Enanthate testosterone 250 mg with two-week intervals

Sponsors

Department of Research & Technology, Ahwaz JundiShapur University of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: inclusion criteria:Symptoms of androgen deficiency;Below normal rang of testosterone;age over 40 years exclusion criteria:

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Erectile dysfunction, Sex Frequency. Timepoint: Baseline , 2 months after the first injection. Method of measurement: International Index of Erectile Function Questionnaire.;Fasting Blood Sugar -2hour post prandial- HemoglobinA1c. Timepoint: Baseline , 2 months after the first injection. Method of measurement: FBS(mg/dl), 2hPP(mg/dl), HbA1C(%).;Cholesterol, Triglyceride , High Density Lipoprotein, Low Density Lipoprotein. Timepoint: Baseline , 2 months after the first injection. Method of measurement: mg/dl.;Blood pressure. Timepoint: Baseline , 2 months after the first injection. Method of measurement: mmhg.

Secondary

MeasureTime frame
Lower urinary tract symptom. Timepoint: Baseline , 2 months after the first injection. Method of measurement: International Prostate Symptom Score.;Depression, Sleep disorders, Fatigue. Timepoint: Baseline , 2 months after the first injection. Method of measurement: BECK QUESTIONNAIR.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaser Abaszade, MD

Ahwaz JundiShapur University of medical sciences

avrinabaszade@yahoo.com+98 46 1233 7926

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026