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

Primary Purpose

Early Stage Endometrial Cancer

Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Upper vaginectomy
Post-operative brachytherapy
Standard procedures
Sponsored by
University Magna Graecia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Early Stage Endometrial Cancer focused on measuring Brachytherapy, Early stage edometrial cancer, Quality of life, Recurrence, Treatment, Vaginectomy

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Early stage endometrial cancer

Exclusion Criteria:

  • Other pre-malignancies and malignancies
  • Major medical conditions
  • Psychiatric disorders
  • Current or past history of acute or chronic physical illness
  • Premenstrual syndrome (PMS)
  • Current or past (within 6 months from study enrolment) use of drugs influencing cognition, vigilance, and/or mood.

Sites / Locations

  • "Pugliese" HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Vaginectomy group

Brachytherapy group

Control group

Arm Description

Upper vaginectomy

Post-operative brachytherapy

Standard treatment

Outcomes

Primary Outcome Measures

Vaginal cuff recurrences

Secondary Outcome Measures

Post-operative complications
Adverse events
Loco-regional recurrence rate
Distant recurrence rate
Quality of life
Overall survival

Full Information

First Posted
July 16, 2008
Last Updated
April 5, 2013
Sponsor
University Magna Graecia
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1. Study Identification

Unique Protocol Identification Number
NCT00719017
Brief Title
Upper Vaginectomy Versus Brachytherapy in Patients With Early Stage Endometrial Cancer Treated With Laparoscopic Surgery
Official Title
Upper Vaginectomy Versus Brachytherapy in Patients With Early Stage Endometrial Cancer Treated With Laparoscopic Surgery: a Randomized Controlled Study.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Unknown status
Study Start Date
September 2007 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
June 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Magna Graecia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Early Stage Endometrial Cancer
Keywords
Brachytherapy, Early stage edometrial cancer, Quality of life, Recurrence, Treatment, Vaginectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Vaginectomy group
Arm Type
Experimental
Arm Description
Upper vaginectomy
Arm Title
Brachytherapy group
Arm Type
Experimental
Arm Description
Post-operative brachytherapy
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Standard treatment
Intervention Type
Procedure
Intervention Name(s)
Upper vaginectomy
Intervention Description
Laparoscopic surgery with upper vaginectomy
Intervention Type
Radiation
Intervention Name(s)
Post-operative brachytherapy
Intervention Description
Laparoscopic surgery followed by brachytherapy
Intervention Type
Procedure
Intervention Name(s)
Standard procedures
Intervention Description
Laparoscopic surgery +/- brachytherapy +/- pelvic radiation
Primary Outcome Measure Information:
Title
Vaginal cuff recurrences
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Post-operative complications
Time Frame
six months
Title
Adverse events
Time Frame
24 months
Title
Loco-regional recurrence rate
Time Frame
24 months
Title
Distant recurrence rate
Time Frame
24 months
Title
Quality of life
Time Frame
24 months
Title
Overall survival
Time Frame
24 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Early stage endometrial cancer Exclusion Criteria: Other pre-malignancies and malignancies Major medical conditions Psychiatric disorders Current or past history of acute or chronic physical illness Premenstrual syndrome (PMS) Current or past (within 6 months from study enrolment) use of drugs influencing cognition, vigilance, and/or mood.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stefano Palomba, MD
Phone
+39-0961.883234
Email
stefanopalomba@tin.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefano Palomba, MD
Organizational Affiliation
Department of Obstetrics and Gynecology, University "Magna Graecia" of Catanzaro
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Fulvio Zullo, MD
Organizational Affiliation
Department of Obstetrics and Gynecology, University "Magna Graecia" of Catanzaro
Official's Role
Study Chair
Facility Information:
Facility Name
"Pugliese" Hospital
City
Catanzaro
ZIP/Postal Code
88100
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ingrid Tomaino, MD
Phone
+39 0961 883234
Email
angela.falbo@libero.it

12. IPD Sharing Statement

Citations:
PubMed Identifier
16202724
Citation
Zullo F, Palomba S, Russo T, Falbo A, Costantino M, Tolino A, Zupi E, Tagliaferri P, Venuta S. A prospective randomized comparison between laparoscopic and laparotomic approaches in women with early stage endometrial cancer: a focus on the quality of life. Am J Obstet Gynecol. 2005 Oct;193(4):1344-52. doi: 10.1016/j.ajog.2005.02.131.
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Upper Vaginectomy Versus Brachytherapy in Patients With Early Stage Endometrial Cancer Treated With Laparoscopic Surgery

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