Under construction – not a live service
Sign in
Not yet taking people in ItalyNo phase

Surgical Handling of Fertility-preserving Treatments for Cervical Adenocarcinomas

Key facts

Where
Roma, ItalySee the site

Where in Italy

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCSRoma, ItalyNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Trial code
NCT07394413
Record updated
6 February 2026
Original description
Despite a growing body of literature on the subject, there is still uncertainty regarding direct comparisons between different conservative surgical techniques for cervical adenocarcinomas. In particular, it remains unclear whether fertility-sparing surgery for cervical adenocarcinomas - characterized by skip lesions - can ensure optimal disease control while achieving adequate obstetric outcomes.Read full original descriptionShow less

Despite a growing body of literature on the subject, there is still uncertainty regarding direct comparisons between different conservative surgical techniques for cervical adenocarcinomas. In particular, it remains unclear whether fertility-sparing surgery for cervical adenocarcinomas - characterized by skip lesions - can ensure optimal disease control while achieving adequate obstetric outcomes.

For this reason, a systematic review and meta-analysis of the literature, along with an analysis of our center's data, is warranted. This approach will allow a critical, comparative evaluation of the efficacy of the different techniques (conization, simple trachelectomy, and radical trachelectomy) and the identification of prognostic factors to guide therapeutic choice.

Inclusion: Adult women of reproductive age with a diagnosis of cervical adenocarcinoma; Undergoing fertility-sparing surgery; Minimum 12-month follow-up; Signed informed consent.

Exclusion: Undergoing radical surgery; Histotypes other than cervical adenocarcinoma; Follow-up less than 12 months.

ClinicalTrials.gov NCT07394413