Oesophageal Cancer Trial, Recruiting NCT01684904 Sponsor: Loma Linda University Condition: Oesophageal Cancer
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Oesophageal Cancer Trial, Recruiting

NCT01684904
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 diagnosed with a confirmed squamous cell or adenocarcinoma (specific types of cancer) of the esophagus (food pipe), affecting the middle, lower, or junction area where the esophagus meets the stomach, with possible stomach involvement of up to 5 cm.
  • People whose cancer has been confirmed through an endoscopy (camera examination of the food pipe) with a tissue biopsy.
  • People whose cancer is at a specific stage (T1N1-2, or T2-3N0-2) based on standard cancer staging guidelines, confirmed through a series of required tests including CT scan, PET scan, and ultrasound examination of the food pipe, all completed within required timeframes before joining.
  • People who have had a recent physical examination with their weight recorded within 30 days of registering for the trial.
  • People whose kidney function blood test results are within an acceptable range within 4 weeks of registration.
  • People whose recent blood tests show the bone marrow is producing enough blood cells (sufficient white blood cells, platelets, and haemoglobin levels).
  • People whose liver function blood test results are within an acceptable range within 4 weeks of registration.
  • People aged 18 or older.
  • People with a general health and activity level rated as acceptable on a standard medical scale (Zubrod performance status 0–2) within 4 weeks of registration.
  • People who have been assessed by a surgeon and confirmed as able to undergo surgery to remove the cancer after completing pre-surgery treatment.
  • Women who could potentially become pregnant must have a negative pregnancy blood test within 14 days before registration.
  • Women who could potentially become pregnant, and male participants, must use adequate contraception throughout the trial.
  • People who have read and signed the trial's informed consent form before entering the study.

Who may not be able to join:

  • People whose esophageal cancer is located in the upper (cervical) part of the food pipe, closest to the throat.
  • People whose cancer is at the very earliest stage (T1N0) or the most advanced local stage (T4).
  • People who have previously received radiation therapy to the chest or as treatment for esophageal cancer.
  • People who have previously received chemotherapy for esophageal cancer.
  • People who have a connection or opening between the food pipe and the airway (tracheoesophageal fistula), or whose cancer has grown into the airway or major breathing tubes.
  • People who have had another type of invasive cancer in the past, unless they have been free of that cancer for at least 2 years (certain very early-stage cancers such as carcinoma in situ of the breast, mouth, or cervix may still be eligible — confirm with trial site).
  • People who have had prior radiation therapy in an area that would overlap with the radiation fields planned for this trial.
  • People who have medical reasons that would prevent them from safely undergoing surgery to remove the esophagus.
  • People who have previously had an allergic reaction to the chemotherapy drugs paclitaxel or carboplatin.
  • People with serious, active other health conditions that may affect survival.
  • Women who are pregnant, breastfeeding, or who could potentially become pregnant, and men who are sexually active and unable or unwilling to use medically acceptable contraception.

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 28 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

Principal Investigator: Gary Yang, MD, gyang@llu.edu

Phone: 909-558-4288 or 1 800 PROTONS

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

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Loma Linda University
Registry
ClinicalTrials.gov
Start date
20 February 2013
Est. completion
1 August 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

To assess overall survival of patients treated with proton-chemotherapy (PCT) followed by surgery in patients with resectable primary esophageal or esophagogastric cancer

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: 28 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