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Recruiting NCT02107105

NCT02107105 Evaluation of Quality of Life and Utilities Following Surgical Treatment of Stage I-IV Rectal Cancer

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Clinical Trial Summary
NCT ID NCT02107105
Status Recruiting
Phase
Sponsor M.D. Anderson Cancer Center
Condition Rectal Adenocarcinoma
Study Type OBSERVATIONAL
Enrollment 430 participants
Start Date 2014-05-16
Primary Completion 2030-05-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Quality-of-Life AssessmentQuestionnaire Administration

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 430 participants in total. It began in 2014-05-16 with a primary completion date of 2030-05-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study evaluates quality of life and utilities following surgical treatment of stage I-IV rectal cancer. This study may help researches learn more about quality of life in patients who have or have had rectal cancer.

Eligibility Criteria

Inclusion Criteria: * Patient has histologically proven adenocarcinoma of the rectum (stage I - IV) that is planned to be treated by surgical resection performed with curative intent, or who has already received surgical treatment * Patient must sign an approved informed consent document and have the literary and physical ability to complete the questionnaire in English Exclusion Criteria: * Patient has been treated with pelvic radiation therapy for a diagnosis other than rectal cancer * Patient has a concurrent cancer diagnosis at the time of consent * Patient has recurrent disease

Contact & Investigator

Central Contact

George Chang

✉ GChang@mdanderson.org

📞 713-792-6940

Principal Investigator

George J Chang

PRINCIPAL INVESTIGATOR

M.D. Anderson Cancer Center

Frequently Asked Questions

Who can join the NCT02107105 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Rectal Adenocarcinoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT02107105 currently recruiting?

Yes, NCT02107105 is actively recruiting participants. Contact the research team at GChang@mdanderson.org for enrollment information.

Where is the NCT02107105 trial being conducted?

This trial is being conducted at Houston, United States.

Who is sponsoring the NCT02107105 clinical trial?

NCT02107105 is sponsored by M.D. Anderson Cancer Center. The principal investigator is George J Chang at M.D. Anderson Cancer Center. The trial plans to enroll 430 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology