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Efficacy and Acceptability of Thermal Ablation in the Treatment of Cervical Neoplasia

Cervical Neoplasm Clinical Trial

Official title:
Efficacy and Acceptability of Thermal Ablation in the Treatment of Cervical Neoplasia

Clinical Trial Summary

Longitudinal study in two referral centers in Morocco to evaluate the effectiveness, the acceptability and safety of thermal ablation in the treatment of cervical neoplasia.

Clinical Trial Description

The study population consisted of women with a positive Visual Inspection with Acetic Acid (VIA) screening test referred for ablative treatment. A total of 119 women with lesions eligible to ablative treatment were counselled and treated by thermal ablation. Informed consent was signed by each participant. Just after treatment, the patients were inquired about the level of pain during the procedure, and their level of satisfaction with the treatment. The women were followed-up at 6 weeks for any complication and re-assessed by colposcopy and biopsy at 12 months for any persistent or recurrent lesion and for any adverse event. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05453318
Study type Interventional
Source International Agency for Research on Cancer
Contact
Status Completed
Phase N/A
Start date October 17, 2017
Completion date August 17, 2020
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