Clinical Trials Directory

Trials / Completed

CompletedNCT01752725

Comparison of BiCision® Versus UltraCision® During Laparoscopic Supracervical Hysterectomy (LASH)

Comparison of BiCision® Versus UltraCision® During Laparoscopic Supracervical Hysterectomy (LASH): A Prospective, Controlled, Randomized, Non-inferiority in Vivo Human Study.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
University Hospital Tuebingen · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of the study is the evaluation of the efficiency and safety of the new, CE-certified thermofu-sion and dissection instrument BiCision® in comparison with the long established Ultracision® Har-monic Scalpel(Ethicon)during a laparoscopic supracervical hysterectomy (LASH).

Conditions

Interventions

TypeNameDescription
DEVICEBiCision®
DEVICEUltracision® Har-monic Scalpel(Ethicon)

Timeline

Start date
2011-10-01
Primary completion
2012-04-01
Completion
2012-04-01
First posted
2012-12-19
Last updated
2012-12-19

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01752725. Inclusion in this directory is not an endorsement.

Comparison of BiCision® Versus UltraCision® During Laparoscopic Supracervical Hysterectomy (LASH) (NCT01752725) · Clinical Trials Directory