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The Effect of Hydrogen Inhalation on the Quality of Life in Patients with Benign Prostatic Hyperplasia

The Effect of Hydrogen Inhalation on the Quality of Life in Patients with Benign Prostatic Hyperplasia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030127
Enrollment
Unknown
Registered
2020-02-23
Start date
2020-03-26
Completion date
Unknown
Last updated
2020-02-25

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

Conditions

Benign Prostatic Hyperplasia

Interventions

Sponsors

Shenzhen Luohu People's Hospital (The Third Affiliated Hospital of Shenzhen University)
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate in the trial and sign a written informed consent form; 2. Aged between 50 and 80 years old (including 50 and 80 years old); 3. Meet the diagnosis of benign prostatic hyperplasia (BPH); 4. QoL score > 3, IPSS between 8 and 19 scores, maximum urinary flow rate < 15ml/s.

Exclusion criteria

Exclusion criteria: 1. Patient has been diagnosed with severe respiratory dysfunction or required oxygen therapy; 2. Patient with serious diseases of other systems such as severe cardiovascular disease, acute stroke, malignant tumor, severe mental illness, etc.; 3. Serum PSA>4 ng/mL; 4. The investigator judges any disease other than benign prostatic hyperplasia that can cause urinary symptoms or changes in urinary flow rate (eg, neurogenic bladder, bladder neck fibrosis, bladder tumor, urinary calculi, urethral stricture, phimosis or penis tumor, acute or chronic prostatitis, prostate cancer, acute and chronic urinary tract infection, acute and chronic renal failure, large (>5 cm) bladder diverticula, etc.); 5. Patient has participated in other clinical trial within 30 days; 6. Poor compliance or fail to complete the test according to the research plan; 7. Other situations that researchers think the patient is not suitable for the research.

Design outcomes

Primary

MeasureTime frame
International Prostate Symptom Score (IPSS);Quality of Life (QoL) Score;Maximum Urinary Flow Rate;

Secondary

MeasureTime frame
Serum creatinine;

Countries

China

Contacts

Public ContactGuixiao Huang

Shenzhen Luohu People's Hospital (The Third Affiliated Hospital of Shenzhen University)

huanggx71@163.com+86 13798304358

Outcome results

None listed

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