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The randomized controlled trial of the curative effect of the CZF single treatment for chronic cervicitis

The randomized controlled trial of the curative effect of the CZF single treatment for chronic cervicitis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10001117
Enrollment
Unknown
Registered
2010-12-01
Start date
2010-04-30
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

Chronic cervicitis

Interventions

Sponsors

National Engineering Research Center of Medical Ultrasound
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Clinical diagnosis of chronic cervicitis; 2. Aged between 20 and 50 years old, married or have sex life for more than three years; 3. Cervical cytology (TBS classification): no intraepithelial neoplasia / malignant cells; 4. With normal Routine blood test results.

Exclusion criteria

Exclusion criteria: 1. Have genital acute or subacute infection; 2. History of hysterectomy and pelvic radiotherapy; 3. History of cervical frozen, cervical electrotherapy, cervical light therapy and other traditional physical therapy and surgical treatment in the past 3 months; 4. In pregnancy, puerperium and menstrual period.

Design outcomes

Primary

MeasureTime frame
The number and size of the cervical polyps;The degree of the cervical hypertrophy;The number and size of the cervical Naboth cyst;Leucorrhea routine examination;The scope and types of the cervical epithelial ectopia;

Secondary

MeasureTime frame
Lumbosacral pain;The amount of Vaginal discharge;With or without bleeding after intercours;

Countries

China

Contacts

Public ContactChengzhi LI
lijiajia5@vip.sina.com+86 13320268972

Outcome results

None listed

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