Outcome After Multidisciplinary CO2 Laser Laparoscopic Excision of Deep Infiltrating Colorectal Endometriosis
NCT ID: NCT00461838
Last Updated: 2009-02-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
56 participants
OBSERVATIONAL
1996-09-30
2004-07-31
Brief Summary
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Detailed Description
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All 56 multidisciplinary operated patients were asked to complete the Oxford Endometriosis Quality of Life questionnaire, a sexual activity questionnaire and visual analogue scales (VAS) for dysmenorroe, chronic pelvic pain and deep dyspareunia, to compare their status before surgery and at the moment of the evaluation (January 2005).
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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1
All women (n=56) who had undergone CO2 laser laparoscopic radical excision of deep infiltrating endometriosis with active involvement of colorectal surgeon and/or urologist were selected retrospectively from the list of all patients (n=more than 2000) operated at the Leuven University Fertility Centre (LUFc) between September 1996 and July 2004.
multidisciplinary laparoscopy
Multidisciplinary (with active involvement of the colorectal surgeon/urologist) fertility-sparing CO2 laser laparoscopic radical excision of deep infiltrating endometriosis.
Questionnaires
Patients (n=56) were asked to complete questionnaires regarding quality of life (QOL), pain, fertility and sexuality to compare their status before and after surgery, and their medical files were analyzed.
Interventions
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multidisciplinary laparoscopy
Multidisciplinary (with active involvement of the colorectal surgeon/urologist) fertility-sparing CO2 laser laparoscopic radical excision of deep infiltrating endometriosis.
Questionnaires
Patients (n=56) were asked to complete questionnaires regarding quality of life (QOL), pain, fertility and sexuality to compare their status before and after surgery, and their medical files were analyzed.
Eligibility Criteria
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Inclusion Criteria
* operated at the Leuven University Fertility Centre (LUFc) between September 1996 and July 2004
Exclusion Criteria
18 Years
45 Years
FEMALE
No
Sponsors
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University Hospital, Gasthuisberg
OTHER
Responsible Party
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University Hospitals Leuven
Principal Investigators
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Christel LC Meuleman, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital Gasthuisberg, Catholic University, Leuven, Belgium
Thomas D'Hooghe, MD, PhD
Role: STUDY_DIRECTOR
University Hospital Gasthuisberg, Catholic University, Leuven, Belgium
Locations
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University Hospital Gasthuisberg
Leuven, , Belgium
Countries
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Other Identifiers
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ML2818 - 22/10/2004
Identifier Type: -
Identifier Source: org_study_id
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