A multi center study on evaluation of different methods for treatment of nonspecific vaginitis effect

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-14005426

Enrollment

Unknown

Registered

2014-03-16

Start date

2015-03-07

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

nonspecific vaginitis

Interventions

A:Baofukang suppository

B:Ozone liquid

C:three percent boric acid

Eligibility

Sex/Gender

Female

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Participate in voluntary with detailed understanding of the purpose of this study and requirements and sign the informed consent; 2. At the age of 18 years old to 65 years old; 3. Non-pregnant females; 4. The clinical diagnosis is non specific vaginitis; 5. No sexual intercourse during treatment or follow-up. Use a condom if she has.

Exclusion criteria

Exclusion criteria: (1) With cervicitis and pelvic inflammatory disease; (2) Using drugs related to the treatment of nonspecific vaginitis; (3) Can't guarantee whether recently she is pregnant or not.

Design outcomes

Primary

Measure	Time frame
sings and symptoms;Drug onset time;Vaginal micro ecological evaluation;	—

Countries

China

Contacts

Public ContactZhaohui Liu; Gengli Zhao

2366216@qq.com+86 13701118639

Outcome results

None listed

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