Skip to content

Analysis of the correlation between stress urinary incontinence in postmenopausal women and serum testosterone and its precursors.

Analysis of the correlation between stress urinary incontinence in postmenopausal women and serum testosterone and its precursors.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300078752
Enrollment
Unknown
Registered
2023-12-18
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

urinary incontinence

Interventions

Urinary incontinence group:Treatment Group: Apply testosterone cream to the vaginal wall, with a dosage of 0.5g each time, twice a week for a total of 10 times. Concurrently, conduct pelvic floor musc
Control group: N/A

Sponsors

Hainan Western central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: Urinary incontinence group: postmenopausal women with clinically diagnosed SUI; Healthy control group: postmenopausal healthy female volunteers recruited during the same period, no benign gynecological diseases, no evidence of stress incontinence and female pelvic floor dysfunction;

Exclusion criteria

Exclusion criteria: 1) had undergone stress incontinence surgery or had a history of stress incontinence surgery, 2) had undergone abdominal or pelvic surgery within the first 6 months of enrolment, 3) had a urinary tract infection, 4) had a history of neurological or psychiatric disorders, 5) had uncertain menopausal status, 6) had been diagnosed with urge incontinence or mixed incontinence, 7) had cancer, 8) had vaginal bleeding with an unknown history, 9) Receiving systemic or local hormone therapy (including oral contraceptives and vaginal estrogen use, ingestion of selective estrogen receptor or androgen receptor modulators), and 10) being unable to read and sign informed consent forms.

Design outcomes

Primary

MeasureTime frame
Serum total testosterone;Serum free testosterone;

Secondary

MeasureTime frame
Sex hormone-binding globulin;Free testosterone/total testosterone ratio;Free testosterone index;Serum deoxyepiandrosterone levels;Serum androstenedione levels;

Countries

China

Contacts

Public ContactYingxiu Chen

Hainan Western central Hospital

chenyingxiu2@126.com+86 182 4511 8305

Outcome results

None listed

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