Development and clinical application of a liquid collection device

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000038601

Enrollment

Unknown

Registered

2020-09-24

Start date

2020-10-01

Completion date

Unknown

Last updated

2020-12-07

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

Conditions

Urinary system diseases

Interventions

Common liquid collector group:Common liquid collector

Common Liquid collector group (urethral opening wipe):Common Liquid collector group and urethral opening wipe

convenient collector group :a convenient collector

convenient collector group (urethral opening wipe):convenient collector group and urethral opening wipe

Eligibility

Sex/Gender

Female

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. The subject is able to read, understand and sign the informed consent; 2. Female subjects aged between 18 and 45 years (including the threshold value) were screened; 3. The subjecthas the ability to move freely.

Exclusion criteria

Exclusion criteria: 1. A history of recurrent urinary tract infection, pelvic organ prolapse, urge urinary incontinence, and stress urinary incontinence; 2. Antibiotics have been used in the last two weeks; 3. Menstruation during screening; 4. Postmenopausal, pregnant or breastfeeding women.

Design outcomes

Primary

Measure	Time frame
Quantity of microbiota;Species of microbial abundance;	—

Countries

China

Contacts

Public ContactXuening Li

li.xuening@zs-hospital.sh.cn+86 13681973906

Outcome results

None listed

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