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Recruiting NCT06295783

NCT06295783 Prospective Evaluation of the Relation Between Different Questionnaires Measuring Radiation-induced Side-effect

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Clinical Trial Summary
NCT ID NCT06295783
Status Recruiting
Phase
Sponsor M.D. Anderson Cancer Center
Condition Radiation
Study Type OBSERVATIONAL
Enrollment 300 participants
Start Date 2024-06-10
Primary Completion 2027-02-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
MDASI-HNEORTC QLQ-C30EORTC HN35

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 300 participants in total. It began in 2024-06-10 with a primary completion date of 2027-02-01.

⚠ 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

To learn more about how you would rate the intensity or severity of your symptoms during or after radiation therapy using questionnaires with different rating scales.

Eligibility Criteria

Inclusion Criteria: * Age ≥18 years * English as a primary language * Participants with a diagnosis of HNC undergoing active curative RT or having received curative RT within the past 5 years at MD Anderson * Ability to complete the survey(s) of their own volition Exclusion Criteria: * Age \< 18 years * Non-English speaking participants * Participants who are receiving or have received RT in a non-HN site. * Participants in follow up and over 5 years from post-treatment * Neurocognitive deficits that render patients unable to complete the survey(s) on their own.

Contact & Investigator

Central Contact

Amy Moreno, MD

✉ akmoreno@mdanderson.org

📞 (713) 745-4590

Principal Investigator

Amy Moreno, MD

PRINCIPAL INVESTIGATOR

M.D. Anderson Cancer Center

Frequently Asked Questions

Who can join the NCT06295783 clinical trial?

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

Is NCT06295783 currently recruiting?

Yes, NCT06295783 is actively recruiting participants. Contact the research team at akmoreno@mdanderson.org for enrollment information.

Where is the NCT06295783 trial being conducted?

This trial is being conducted at Houston, United States.

Who is sponsoring the NCT06295783 clinical trial?

NCT06295783 is sponsored by M.D. Anderson Cancer Center. The principal investigator is Amy Moreno, MD at M.D. Anderson Cancer Center. The trial plans to enroll 300 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: September 2026  ·  Data Methodology