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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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Netherlands Trial Register |
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Last refreshed on:
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28 April 2013 |
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Main ID: |
NTR964 |
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Date of registration:
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01/05/2007 |
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Primary sponsor: |
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Public title:
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Hemostasis with vesselsealinstrument compared to conventional bipolar coagulation in laparascopic hysterectomy and/or salpingo-ooforectomy. a randomised trial
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Scientific title:
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N/A - N/A |
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Date of first enrolment:
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1/1/2007 |
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Target sample size:
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144 |
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Recruitment status: |
recruiting |
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URL:
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http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=964 |
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Study type:
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intervention |
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Study design:
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Randomised: Yes; Masking: None; Control: Active; Group: Parallel; Type: -
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Countries of recruitment
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The Netherlands
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Contacts
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Name:
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H.A.M.
Brölmann |
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Address:
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VU University Medical Center
De Boelelaan 1117
Amsterdam
The Netherlands |
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Telephone:
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+31 20 4444851 |
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Email:
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h.brolmann@vumc.nl |
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Affiliation:
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Name:
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H.A.M.
Brölmann |
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Address:
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VU University Medical Center
De Boelelaan 1117
Amsterdam
The Netherlands |
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Telephone:
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+31 20 4444851 |
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Email:
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h.brolmann@vumc.nl |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: 1. Laparoscopic hysterectomy;
2. Laparoscopic oophorectomy
Exclusion criteria: 1. Ovarian or cervical cancer;
2. Uterus size > 20 weeks pregnancy
Age minimum:
Age maximum:
Gender:
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Health Condition(s) or Problem(s) studied
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Vesselseal, Laparoscopy, Hysterectomy, Ovariectomy
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Intervention(s)
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Hemostasis with vesselseal technique
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Primary Outcome(s)
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1. Operating time;
2. Intraoperative bloodloss
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Secondary Outcome(s)
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1. Hemoglobin drop;
2. User satisfaction;
3. Costs;
4. Quality of life (SF36)
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Secondary ID(s)
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ISRCTN80747160
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Source(s) of Monetary Support
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