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Efficacy and safety of cryotherapy in comparison with Chinese herbal medicine in the treatment of chronic cervicitis and cervical erosio

Phase 3
Conditions
Chronic cervicitis.
Inflammatory disease of cervix uteri
Registration Number
IRCT201512107265N4
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
70
Inclusion Criteria

Developing chronic cervicitis or cervical erosion; Papanicolaou smear class 1 or 2; Normal colposcopy.
Exclusion criteria: Papanicolaou smear indicating papilloma or CIN; Sensitivity to plastic materials; Cervical prolapse greater than grade 1

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The degree of cervicitis. Timepoint: Before intervention, 48 hours after the intervention, one week after the intervention, 3 days after the end of the next menstruation and at weeks 6 and 12. Method of measurement: clinical examination of cervix (observation) and recording in the study check list.
Secondary Outcome Measures
NameTimeMethod
Complications. Timepoint: 48 hours after the intervention, one week after the intervention, 3 days after the end of the next menstruation and at weeks 6 and 12. Method of measurement: questionnaire.;Time to treatment response. Timepoint: Before intervention, 48 hours after the intervention, one week after the intervention, 3 days after the end of the next menstruation and at weeks 6 and 12. Method of measurement: clinical examination of cervix (observation) and recording in the study check list.
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