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Main
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Note: This record shows only 22 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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German Clinical Trials Register |
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Last refreshed on:
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8 April 2024 |
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Main ID: |
DRKS00009904 |
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Date of registration:
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11/08/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Incidence and reasons for dehiscence of sutures after total laparoscopic hysterectomy
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Scientific title:
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Incidence and reasons for dehiscence of sutures after total laparoscopic hysterectomy - - |
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Date of first enrolment:
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01/03/2016 |
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Target sample size:
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450 |
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Recruitment status: |
Complete |
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URL:
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http://drks.de/search/en/trial/DRKS00009904 |
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Study type:
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observational |
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Study design:
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Allocation: ; Masking: ; Control: ; Assignment: ; Study design purpose: other
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Phase:
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Countries of recruitment
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Germany
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Contacts
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Name:
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Julia
Radosa |
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Address:
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Kirrberger Straße, Gebäude 9
66421
Homburg
Germany |
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Telephone:
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068411628101 |
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Email:
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julia.radosa@uks.eu |
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Affiliation:
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Universitätsfrauenklinik Homburg |
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Name:
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Julia
Radosa |
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Address:
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Kirrberger Straße, Gebäude 9
66421
Homburg
Germany |
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Telephone:
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068411628101 |
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Email:
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julia.radosa@uks.eu |
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Affiliation:
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Universitätsfrauenklinik Homburg |
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Key inclusion & exclusion criteria
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Inclusion criteria: Hysterektomy in patients with benign uterine pathology
Exclusion criteria: Hysterektomy in patients with malign uterine pathology
Age minimum:
18 Years
Age maximum:
None
Gender:
Female
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Health Condition(s) or Problem(s) studied
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D25.9
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Leiomyoma of uterus, unspecified
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D25.9
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Intervention(s)
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Group 1: Observation of perioperative risk factors after laparoscopic hysterectomy like blood loss, time of surgery, former surgeries, suture technique or experience of the surgeon as potential risk factors for suture insufficience
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Primary Outcome(s)
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Assessment of patient history as well as patient interviews of 450 patients after laparoscopic hysterectomy to evaluate perioperative risk factors of suture insufficience
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Secondary Outcome(s)
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Prevention of dehiscence
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Source(s) of Monetary Support
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Universitätsfrauenklinik Homburg Kirrbergerstraße 66421 HomburgFinanzierung über die HOMFOR-Förderung
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Ethics review
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Status: No approval required according to the EC
Approval date: 29/02/2016
Contact:
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