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Tissue Sparing Therapy of Female Precancerous Genital Lesions With VITOM

Not Applicable
Conditions
Cervical Preinvasive Disease
Interventions
Device: Colposcopy
Device: Vitom
Registration Number
NCT01601769
Lead Sponsor
Charite University, Berlin, Germany
Brief Summary

Object of the study is the evaluation of the use of a rigid laparoscope for the diagnosis and therapy of lesions of the female genital tract as a substitution or a complementary method to colposcopy with the development of new standards for a tissue sparing therapy Use of existing laparoscopic instruments, which allow a better quality level in the diagnosis and therapy than the current routine.

Development of new optics and instruments, which allow a tissue sparing approach Pre and postoperative measurement of the cervical volume, to be sure that the tissue removal is kept to a minimum level Development of qualitaty parameters for the most tissue respecting operations of the uterine cervix Prospective evaluation of the influence of tissue sparing surgery on future pregnancies

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
300
Inclusion Criteria
  • Karnowsky-Index > 80,
  • 18-80 years,
  • CIN.
Exclusion Criteria
  • Pregnancy,
  • Previous or current cancer,
  • Radio therapy of the pelvis,
  • Serious internistic accompanying diseases,
  • Psychiatric diseases,
  • HIV infection,
  • Drug addiction.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ColposcopyColposcopya Carl Zeiss colposcope with a magnification power from 4x to 20x, with green filter.
VitomVitomThe VITOM system, consisting of the VITOM scope, xenon light source, HD camera system, AIDA HD documentation system, 1 monitor, and a mechanical support arm (all Karl Storz, Tuttlingen, Germany) is used for video exocolposcopy.
Primary Outcome Measures
NameTimeMethod
Cervical volume removedİmmediately after surgery

Cervical volume removed during the operation is recorded

İntraoperative ComplicationsDuring the intraoperative

Complications encountered during the prodecure

Short term complicationsWithin 48 hours after operation

Complications within 48 hours after operation

Late complicationsAfter 48 hours

Complications occuring after 48 hours

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Charité University Hospital

🇩🇪

Berlin, Germany

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