Contributing Factors to Anterior Resection Syndrome and Its Impact on Quality of Life: A Retrospective Cohort Study
NCT ID: NCT04114591
Last Updated: 2019-10-03
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
179 participants
OBSERVATIONAL
2018-07-01
2019-01-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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LARS symptoms
Patient suffering from LARS as identified through LARS questionnaire
anterior resection
The distance from anal verge, preoperative radiotherapy and presence of stoma were analysed
No LARS symptoms
Absence of LARS symptoms
anterior resection
The distance from anal verge, preoperative radiotherapy and presence of stoma were analysed
Interventions
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anterior resection
The distance from anal verge, preoperative radiotherapy and presence of stoma were analysed
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* permanent stoma
* known disseminated or recurrent disease,
* patient without restitution of bowel continuity after 1 year
18 Years
ALL
No
Sponsors
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University of Malta
OTHER
Responsible Party
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Svetlana Doris Brincat
Surgical trainee
Principal Investigators
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Svetlana Doris Brincat
Role: PRINCIPAL_INVESTIGATOR
Mater Dei Hospital
Locations
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Mater Dei Hospital
Valletta, , Malta
Countries
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Other Identifiers
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S07/18
Identifier Type: -
Identifier Source: org_study_id
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