Head and Neck Cancer Trial, Recruiting NCT05872880 Sponsor: Xiangya Hospital of Central South University Condition: Head and Neck Cancer
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Head and Neck Cancer Trial, Recruiting

NCT05872880
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People with a general health and activity level rated as fully active or restricted only in strenuous physical activity (as measured by a standard oncology performance scale).
  • People newly diagnosed with squamous cell carcinoma (a specific type of cancer) of the mouth lining, confirmed by a tissue biopsy.
  • People whose cancer is located in one of these areas: the tongue (main body), floor of the mouth, gums, inner cheek lining, hard palate (back portion), or the molar region.
  • People whose cancer is at an intermediate to advanced stage (Stage III to IVB), based on standard cancer staging assessments.
  • People whose tumor has been assessed by doctors as able to be fully surgically removed, either now or after an initial course of treatment to shrink it.
  • People who are well enough to tolerate the planned treatments, have no medical reasons preventing surgery, and whose scans (chest CT, bone scan, or PET-CT) show the cancer has not spread to distant parts of the body.
  • Women of childbearing age (15–49 years old) who have a negative pregnancy test taken within 7 days before treatment begins, and all participants who are able to have children must agree to use effective contraception throughout the trial and for three months after finishing treatment.
  • People who have voluntarily signed a consent form and are willing and able to attend follow-up appointments and meet all other study requirements.

Who may not be able to join:

  • People who have previously received cancer treatments such as chemotherapy, radiation therapy, or immunotherapy for this condition.
  • People who decline to sign the informed consent form.
  • People who are unwilling to accept the treatment options in the study, or who are unable to complete treatment or attend regular follow-up appointments due to psychological, social, family, or geographical reasons.
  • People with a known allergy to any of the drugs that may be used in this trial.
  • People whose general health is too poor to tolerate treatment — for example, if routine blood tests show that haemoglobin, white blood cell count, or platelet levels are below certain thresholds, or if kidney function markers are above a certain level (confirm specific values with the trial site).
  • People whose cancer stage does not meet the trial requirements — for example, those with very early-stage oral cancer (T1–2N0) or those whose cancer has already spread to distant parts of the body (M1).
  • People whose cancer cannot be surgically removed because it has grown into critical structures such as major blood vessels (e.g., the carotid artery) or vital areas of the brain.
  • Women who are pregnant or breastfeeding.
  • People who currently have, or have previously had, another type of cancer — with the exception of certain adequately treated skin cancers, cervical carcinoma in situ, or papillary thyroid carcinoma.
  • People who have participated in another clinical trial within the past 30 days.
  • People with serious illnesses (including mental illness), severely abnormal test results, or other social or personal factors that researchers determine could affect their safety or ability to complete the study.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 22 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 1817313127

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Xiangya Hospital of Central South University
Registry
ClinicalTrials.gov
Start date
1 April 2022
Est. completion
1 March 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-free survival; Objective response rate; Major partial response

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov