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Clinical Trials/NCT04114591
NCT04114591
Completed
Not Applicable

Contributing Factors to Anterior Resection Syndrome and Its Impact on Quality of Life: A Retrospective Cohort Study

University of Malta1 site in 1 country179 target enrollmentJuly 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Anterior Resection Syndrome
Sponsor
University of Malta
Enrollment
179
Locations
1
Primary Endpoint
LARS incidence
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This study adds to the understanding of the contributing factors leading to LARS, the long term effects of this syndrome post-operatively and its impact on quality of life.

Registry
clinicaltrials.gov
Start Date
July 1, 2018
End Date
January 30, 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Svetlana Doris Brincat

Surgical trainee

University of Malta

Eligibility Criteria

Inclusion Criteria

  • All adult patients \>18 years, under the care of all surgical firms at Mater Dei Hospital, who had undergone anterior resection for rectal cancer between January 2014 and December 2016

Exclusion Criteria

  • colorectal cancer (\>15cm) from anal verge
  • permanent stoma
  • known disseminated or recurrent disease,
  • patient without restitution of bowel continuity after 1 year

Outcomes

Primary Outcomes

LARS incidence

Time Frame: 1 year

Incidence of LARS in patients who had anterior resection

Life

Time Frame: 1 year

The association between LARS and quality of life was assessed.

Risk factors

Time Frame: 1 year

Variable factors which might have contributed to LARS were the following: * Age * Gender * Diabetes mellitus * Pathological stage * MRI stage * Distance from anal verge * Surgical technique * Preoperative radiotherapy * Preoperative chemotherapy * Postoperative radio/chemotherapy * Type of anastomosis * Presence of stoma * Interval from stoma reversal * Duration of follow-up

Study Sites (1)

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