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New Use of the ViKY Device for Uterus Positioning

NCT01531504 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2012-12-28

No results posted yet for this study

Summary

Evaluation of Safety and Efficacy of ViKY Device for Uterus Positioning on 2 US sites

Conditions

  • Surgical Procedure, Unspecified

Interventions

DEVICE

ViKY UP

laparoscopic-assisted hysterectomy procedure

Sponsors & Collaborators

  • EndoControl

    lead INDUSTRY

Principal Investigators

  • Arnold ADVINCULA, MD · Floridal Hospital

  • Kevin STEPP, MD · Carolinas Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2012-08-31
Completion
2012-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01531504 on ClinicalTrials.gov