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Validation of Low Anterior Resection Syndrome Score in Korean Version

Validation of Low Anterior Resection Syndrome Score in Korean Version

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03211715
Enrollment
300
Registered
2017-07-07
Start date
2017-07-19
Completion date
2018-12-31
Last updated
2017-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neoplasm of Rectum, Surgery, Surgery--Complications

Brief summary

In contemporary era of rectal cancer treatment, development of surgical technique and tool, adaptation of chemoradiation therapy, as well as multidisciplinary approach have led increased survival as well as rate of sphincter preservation. However, poor anorectal function, such as fecal incontinence and/or urgency, has also been increased. Such anorectal dysfunction is named as low anterior resection syndrome, and its rate has been reported in 40 to 90% in rectal cancer patients who received sphincter preserving surgery. Low anterior resection syndrome is known to debilitate quality of life in survivors of rectal cancer. Previously, several studies attempted to evaluate the low anterior resection syndrome via questionnaires and scoring system. Adapting the low anterior resection syndrome score system created in Denmark, this study investigates the validity of the scoring system in Korean language.

Detailed description

In this study, the low anterior resection syndrome score questionnaire proposed by Therese Juul is translated to Korean language by 3 different professional translators. Patients who received sphincter saving surgery to treat rectal cancer will be asked to fill up the questionnaire. Compiling the results, the quality of life after sphincter preserving surgery will be investigated in the association with the low anterior resection syndrome.

Interventions

OTHERquestionnaire

Rectal cancer patients who received sphincter saving surgery will be asked to fill up questionnaire related to bowel dysfunction

Sponsors

Saint Vincent's Hospital, Korea
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

* age 20-80 * surgery undertook from Jan. 2009 to Dec. 2016 * diagnosed with adenocarcinoma * curative intent of surgery * planned surgery * sphincter saving surgery

Exclusion criteria

* patients with stage IV * emergency surgery * patients with recurrent disease

Design outcomes

Primary

MeasureTime frameDescription
Quality of life in association to the severity of bowel dysfunction3 months follow-up, 6 months follow-up, 1 year follow-up, 2 year follow-up, 3 year follow-up, 4 year follow-up, 5 year follow-up, beyond 5 year follow-upThe change in the quality of life will be evaluated based on the questionnaire in regard to bowel dysfunction

Contacts

Primary ContactRi Na Yoo, MD
ninayoo1111@gmail.com82-10-2531-0605
Backup ContactHyungjin Kim, MD, Ph.D
hj@catholic.ac.kr82-249-7170

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026