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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06359730
Other study ID # 253/26-March-2024
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2017
Est. completion date December 1, 2022

Study information

Verified date April 2024
Source Zagazig University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Sphincter sparing surgery is oftentimes associated with bowel dysfunction complaints, namely the low anterior resection syndrome (LARS). The LARS questionnaire is widely used to assess this syndrome. With advances in colorectal surgery, sparing sphincter surgeries are gaining popularity. But symptoms after surgery can affect the quality of life which has psychomotor effects. Low anterior resection syndrome score is a worldwide known questionnaire. Many countries have accredited validation and translation of this questionnaire, but to our knowledge; it is the first time in Egypt.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date December 1, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Age more than 18 - Diagnosed patients with rectal adenocarcinoma and who received low anterior resection with anastomosis creation or after a minimum 6 months interval after stoma reversal. - Tumors of the rectum (2-15 cm) from anal verge Exclusion Criteria: - • cognitive dysfunction - Having a history of inflammatory bowel disease or any disease with bowel function impairment namely, Crohn's disease, irritable bowel syndrome, ulcerative colitis or others. - Age less than 18 - Metastatic cancer or tumor recurrence - Rectal tumors within 2 cm from anal verge( abdominoperineal)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
LARS score questionnaire
LARS score questionnaire is filled by the patient after anterior resection for rectal cancer to study the quality of life

Locations

Country Name City State
Egypt Zagazig University Hospitals Zagazig

Sponsors (1)

Lead Sponsor Collaborator
Zagazig University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary age age of the patients in years was recorded from patient records from 2017 to 2022
Primary sex sex of patients was recorded from patient records from 2017 to 2022
Primary medical disease medical disease like diabetes and hypertension was recorded from patient records from 2017 to 2022
Primary site of tumor tumor site was determined in Cm from anal verge by colonoscopy from 2017 to 2022
Primary neoadjuvant therapy history of neoadjuvant therapy before surgery was obtained from patients records from 2017 to 2022
Primary site of anastmosis site of anastmosis after resection was recorded as colo-rectal or colo-anal from 2017 to 2022
Primary type of meso-rectal excision excision of meso-rectum was recorded if it was partial or complete from 2017 to 2022
Primary adjuvant therapy it was recorded from patients records if he\she had chemo- or radiotherapy post-operatively from 2017 to 2022
Primary type of surgery from records; surgery was open or laparoscopic from 2017 to 2022
Primary type of anastmosis type of anastmosis(hand sewen or stappled) obtained from records from 2017 to 2022
Primary LARS score obtained by LARS questionnaire filled by the patient during follow up, it was formed of five questions with different scores on answer choices, interpretaion (0-20) means no LARS, (21- 29) means minor LARS, (30-42) means major LARS from 2017 to 2022
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