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Risk factors of vulvovaginal candidiasis among women of reproductive age in Xi’an: A cross-sectional study

Risk factors of vulvovaginal candidiasis among women of reproductive age in Xi’an: A cross-sectional study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
TCTR
Registry ID
TCTR20180226005
Enrollment
Unknown
Registered
2018-02-26
Start date
2016-04-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

to analyze the risk factors of VVC among women of reproductive age

Interventions

Ninety&#45
seven patients with VVC were attributed to the case group,Eighty&#45
seven women who underwent routine gynecological examination and had normal vaginal microflora were recruited in the control group.
Prevention,Prevention

Sponsors

An Ruifang
Lead Sponsor
Zeng Xianling,Zeng Xianling
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1)18-50 years old with a history of sexual life; (2)diagnosed with simple VVC or normal vaginal microflora; (3)menstruation ends for at least 3 days, no vaginal irrigation or drug delivery in the vagina within 7 days and no sexual intercourse within 3 days before examination.

Exclusion criteria

Exclusion criteria: Exclusion criteria: Women who had mixed vaginitis; women who was in the period of pregnancy, menstruation or lactation; women who had hysterectomy or bilateral excision of the appendix. Besides, patients with incomplete medical record were also excluded.

Design outcomes

Primary

MeasureTime frame
Univariate analysis of general information and daily living habits. 31/01/2017 face to face questionnaire survey

Secondary

MeasureTime frame
Univariate analysis of hygienic habits. 31/05/2017 face to face questionnaire survey

Countries

China

Contacts

Public ContactRuifang An

xi'an jiaotong university

anruifang@xjtu.edu.cn029-85323844

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026