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Effect Of Testosterone Supplements On Anemia And Quality Of Life Amongst Patients On Regular Hemodialysis

Effect Of Testosterone Replacement On Anemia And Quality Of Life Amongst Patients On Maintenance Hemodialysis

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624001137583
Enrollment
160
Registered
2024-09-20
Start date
2024-01-01
Completion date
2024-01-15
Last updated
2026-05-04

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

Conditions

None listed

Brief summary

My research focuses on relationship between testosterone replacement and its effects on anaemia and quality of life amongst patients on hemodialysis

Interventions

Injection testosterone enanthate 250mg subcut will be given once fortnightly for 6 months it will be administered by a dialysis nurse 30 mins after each dialysis session. Adherence would be ensured as it will be administered and documented by a dialysis nurse.

Sponsors

Dr Qurat Ul Ain Azam - Pak Emirates Military Hospital
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Patients diagnosed with end-stage renal disease (ESRD) requiring maintenance hemodialysis. 2. Patients with documented anemia, defined as haemoglobin levels < 10 g/dL 3. Patients with stable medical conditions, defined as absence of acute illness or major surgical procedures within the past three months. 4. Patients who have been on a stable hemodialysis regimen for at least three months prior to enrollment.

Exclusion criteria

1. Patients with known hypersensitivity or contraindications to testosterone replacement therapy (TRT). 2. Patients with active malignancy, including prostate cancer. 3. Patients with uncontrolled hypertension (systolic blood pressure > 180 mmHg or diastolic blood pressure > 110 mmHg). 4. Patients with severe liver disease (e.g., cirrhosis) or severe hepatic dysfunction (e.g., Child-Pugh class B or C). 5. Patients with severe cardiac disease (e.g., congestive heart failure, recent myocardial infarction) or unstable cardiovascular conditions. 6. Patients with a history of thromboembolic events (e.g., deep vein thrombosis, pulmonary embolism). 7. Patients with significant psychiatric illness or cognitive impairment that may affect their ability to participate in the study or provide informed consent.

Outcome results

None listed

Source: ANZCTR · Data processed: May 7, 2026