Viewing Study NCT01436903


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Study NCT ID: NCT01436903
Status: COMPLETED
Last Update Posted: 2013-03-08
First Post: 2011-08-12
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Chances for Success of CavatermTM Surgery as a Function of Uterus Probe Length
Sponsor: Medical University of Vienna
Organization:

Study Overview

Official Title: Chances for Success of CavatermTM Surgery as a Function of Uterus Probe Length, a Questionnaire Investigation on 290 Patients
Status: COMPLETED
Status Verified Date: 2013-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: CavatermTM is a second-generation thermal balloon ablation device in the management of menorrhagia. The purpose of this study is to investigate the success (questionnaire) of CavatermTM dependent on uterus probe length, especially corpus probe length, which is measured during surgery.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: