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Clinical Trial Summary

Trichloroacetic acid 85% =TCA is an investigational device intended to achieve a complete histologic remission in individuals with cervical intraepithelial neoplasia (CIN) grade 1/2. The device system is to be used only in accordance with the approved Investigational Plan on subjects, who have given written informed consent. High remission and regression rates are expected after a single topical treatment with 85% TCA. After a single topical treatment with 85% TCA for CIN 1-2 (Expected 70% or higher; null hypothesis: not higher than 55%). Regression is defined as improvement from high grade lesion (CIN 2) at baseline to low grade lesion (CIN 1) after TCA treatment. Regression from CIN 1 normal squamous epithelium after the TCA treatment is equal to remission and will be counted as a remission in combined analysis. Remission is defined as complete histologic remission of CIN back to normal squamous epithelium after the TCA treatment, i.e., no cervical dysplasia is detectable by histology or cytology after the TCA treatment. Type-specific HPV Clearance is defined as disappearance of the HPV type detected at screening.


Clinical Trial Description

Visit and assessment Schedule: Visit1 Screening: - Informed Consent, - Inclusion/Exclusion Criteria, - Medical History, - Gynecological Examination - Cytology - HPV Test - Colposcopy - Biopsy - VAS (Visual analog scale) - Pregnancy test Visit 2 Treatment Day with TCA 85%: - Colposcopy - TCA Treatment - VAS - Pregnancy test Visit 3, Control 1, Week 10-14: - Cytology - HPV Test - Colposcopy - Biopsy - 4-quadrant biopsy - ECC - Adverse event monitoring If there is no sign of CIN during the colposcopic examination 10-14 weeks a 4-quadrant biopsy and a ECC are performed Visit 4, Control 2, Week 22-26: - Cytology - HPV Test - Colposcopy - Biopsy - 4-quadrant biopsy - ECC - Adverse event monitoring - Pregnancy test If there is no sign of CIN during the colposcopic examination 22-26 weeks after the TCA treatment, a 4-quadrant biopsy and a ECC are performed. Visit 5, EOS , Week 24-30: - Results Discussion ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04400578
Study type Interventional
Source Krankenhaus Barmherzige Schwestern Linz
Contact
Status Completed
Phase N/A
Start date February 7, 2020
Completion date January 18, 2022

See also
  Status Clinical Trial Phase
Recruiting NCT05624827 - The Role of FAM19A4 and Hsa-mir-124 Methylation in Predicting Prognosis of Untreated Cervical Intraepithelial Neoplasia 2 (CIN 2) N/A
Not yet recruiting NCT06403618 - Evaluation of the PreCursor-M+® in CIN2
Terminated NCT00005808 - Photodynamic Therapy Using Lutetium Texaphyrin in Treating Patients With Cervical Intraepithelial Neoplasia Phase 1
Withdrawn NCT01313104 - Colposcopy and High Resolution Anoscopy in Screening For Anal Dysplasia in Patients With Cervical, Vaginal, or Vulvar Dysplasia or Cancer N/A