Clinical application of new silicone foley catheter: a randomized controlled trial

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100052538

Enrollment

Unknown

Registered

2021-10-30

Start date

2021-11-01

Completion date

Unknown

Last updated

2022-10-17

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

Conditions

catheterization

Interventions

experimental group:insert the silicone foley cathether

control group:traditional disposable catheter

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1. Select the pregnant women who delivered in the hospital; 2. The pregnant women who need indwelling catheter within 24 hours; 3. Pregnant women and their families agreed our study.

Exclusion criteria

Exclusion criteria: 1. The pregnant women who had medical dispute or nursing risks; 2. The pregnant women who had urinary tract infection before opreation; 3. The pregnant women who had other complpications that can not join our study.

Design outcomes

Primary

Measure	Time frame
Bacterial Growth;	—

Countries

China

Contacts

Public ContactJiang Bo

Huairou Maternal and Child Health Care Hospital, Beijing Obsterics and Gynecology Hospital, Capital Medical University

963944231@qq.com+86 13716753060

Outcome results

None listed

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