Pain Related Sexual Dysfunction After Laparoscopic Inguinal Hernia Repair
NCT ID: NCT01086007
Last Updated: 2015-10-30
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
1172 participants
OBSERVATIONAL
2010-02-28
2010-06-30
Brief Summary
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The investigators want to assess this problem among patients after laparoscopic inguinal hernia repair with(self-administered questionnaire study).
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Detailed Description
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Conditions
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Study Groups
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Pain patients
Patients with pain related sexual dysfunction after laparoscopic inguinal hernia repair
No interventions assigned to this group
Non-pain patients
Patients with no pain related sexual dysfunction after laparoscopic inguinal hernia repair
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* \>18 yrs
Exclusion Criteria
18 Years
50 Years
MALE
No
Sponsors
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Innovative Medicines Initiative
OTHER
Rigshospitalet, Denmark
OTHER
Responsible Party
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Gitte Linderoth
MD
Principal Investigators
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Gitte Linderoth, MD
Role: PRINCIPAL_INVESTIGATOR
Section of Surgical Pathophysiology, Rigshospitalet
Locations
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Section of Surgical Pathophysiology, Rigshospitalet
Copenhagen East, , Denmark
Countries
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Other Identifiers
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H-2-2009-126-B
Identifier Type: -
Identifier Source: org_study_id
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