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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05445245
Other study ID # 202101979B0
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date April 14, 2022
Est. completion date February 28, 2025

Study information

Verified date February 2024
Source Chang Gung Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aims are to identify the trajectory of LAR Syndrome and explore the adaptation process and coping strategies of LAR Syndrome in patients newly diagnosed with rectal cancer. The participants will recruit from a CRC surgical outpatient department of a medical center in northern Taiwan.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 80
Est. completion date February 28, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: 1. Patients with stage I to III rectal cancer. 2. Patients already know their condition. 4. Aged 20 years and older. 5. Consciously communicate in Mandarin or Taiwanese. 6. Agreed with the interview and had signed the permit. Exclusion Criteria: 1. Patients with Stage IV rectal cancer. 2. Recurred rectal cancer.

Study Design


Locations

Country Name City State
Taiwan Chung Gung University Taoyuan City Kwei-Shan Dist.

Sponsors (1)

Lead Sponsor Collaborator
Chang Gung Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Self-report Questionnaire show the specific trajectory of LAR Syndrome, psychological distress, and fecal incontinence-related QoL based on different tumor locations in patients with rectal cancer Change from baseline symptom at 12 months
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