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Use of the Enseal Intrument for Laparoscopic Supracervical Hysterectomy

NCT01806012 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2013-03-06

No results posted yet for this study

Summary

The use of the EnSeal® instrument for laparoscopic supracervical hysterectomy in a randomized, single-blinded comparison to the conventional procedure. The objective of the study is to investigate if the use of the Enseal sealing instrument for supracervical hysterectomy leads to a shortening of the operation time.

Conditions

  • Indications for Laparoscopic Supracervical Hysterectomy

Interventions

DEVICE

Sealing tissue with the Enseal device

PROCEDURE

Conventional supracervical hysterectomy

Sponsors & Collaborators

  • Ethicon Endo-Surgery (Europe) GmbH

    collaborator INDUSTRY

  • University Hospital Tuebingen

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-08-31
Primary Completion
2011-08-31
Completion
2011-08-31

Countries

  • Germany

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 NCT01806012 on ClinicalTrials.gov