Clinical Trials Directory

Trials / Unknown

UnknownNCT00719017

Upper Vaginectomy Versus Brachytherapy in Patients With Early Stage Endometrial Cancer Treated With Laparoscopic Surgery

Upper Vaginectomy Versus Brachytherapy in Patients With Early Stage Endometrial Cancer Treated With Laparoscopic Surgery: a Randomized Controlled Study.

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
University Magna Graecia · Academic / Other
Sex
Female
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Recent findings have suggested that laparoscopic surgery is safe and effective, as well as laparotomic one, for treating patients with early stage endometrial cancer (ESEC). Moreover, our long-term previous data have shown a trend in vaginal cuff recurrence in subjects who underwent laparoscopic approach to ESEC consisting of extrafascial hysterectomy, bilateral salpingo-oophorectomy, pelvic +/- para-aortic nodes dissections, regardless grading or lymphovascular space invasion. Based on these considerations, the aim of the current protocol-study will be to compare two different strategies for vaginal cuff recurrences prevention in patients affected by ESEC treated with laparoscopic surgery. In particular, upper vaginectomy followed by observation will be compared to post-operative brachytherapy.

Detailed description

Women with ESEC scheduled for laparoscopic surgery will be enrolled and randomized in three arms \[vaginectomy group (VG), brachytherapy group (BG), and control group (CG)\]. All laparoscopic procedures will consist of total hysterectomy, bilateral salpingo-oophorectomy, peritoneal washing, systematic inspection of peritoneal cavity and biopsy of each suspect lesion, and pelvic (and eventual para-aortic) lymphadenectomy. In VG an upper vaginecomy will be added to standard laparoscopic procedures followed by observation, whereas BG will receive post-operative brachytherapy. CG will be treated with standard protocol for management of ESEC according to National Comprehensive Cancer Network (www.nccn.org). Safety and efficacy data will be recorded in each group for 24 months of follow-up. Data will be analyzed using the intention-to-treat principle and a P value of 0.05 or less will be considered significant.

Conditions

Interventions

TypeNameDescription
PROCEDUREUpper vaginectomyLaparoscopic surgery with upper vaginectomy
RADIATIONPost-operative brachytherapyLaparoscopic surgery followed by brachytherapy
PROCEDUREStandard proceduresLaparoscopic surgery +/- brachytherapy +/- pelvic radiation

Timeline

Start date
2007-09-01
Primary completion
2013-12-01
Completion
2014-06-01
First posted
2008-07-21
Last updated
2013-04-08

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT00719017. Inclusion in this directory is not an endorsement.