PULSO Trial: Pulsed Low-Dose-Rate Radiation for Esophageal Cancer
This study, called the PULSO Trial, is looking at a new way to give radiation therapy for esophageal cancer. It compares standard radiation therapy with a technique called Pulsed Low-Dose-Rate (PLDR) radiation. PLDR radiation delivers the same total dose but in small pulses with pauses in between, which may be less harmful to healthy tissues while still killing cancer cells. Participants will also receive chemotherapy, either modified FLOT or modified FOLFOX-6 before radiation, and carboplatin/paclitaxel weekly during radiation. The study wants to see if PLDR radiation leads to fewer problems like difficulty swallowing (esophagitis) during and after treatment. You may be able to join if you are 18 or older and have Stage II-IVb adenocarcinoma of the esophagus. The study is currently unclear on its recruitment status and plans to enroll 50 people.
- Study design
- This is a Phase 2, prospective, randomized, open-label study comparing two radiation approaches. It plans to enroll 50 participants.
- What's involved
- Participants will receive 2-4 months of induction chemotherapy, followed by chemoradiation therapy. Surgery may also be part of your treatment plan.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study will track new or increased narcotic prescriptions and oral intake for up to 6 weeks after radiation treatment.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
PULSO Trial: Pulsed Low-Dose-Rate (PLDR) Radiation Chemoradiation (CRT) vs. Standard CRT for Esophageal Cancer
At a glance
Conditions
NCT06906887
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Froedtert & the Medical College of Wisconsin
Milwaukee, Wisconsinstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Lindsay Puckett, MD · PRINCIPAL_INVESTIGATOR · Medical College of Wisconsin
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- New prescription for narcoticsUp to 6 weeks after radiation treatment
The number of subjects requiring a new prescription for narcotics.
- Increasing existing narcoticsUp to 6 weeks after radiation treatment
The number of subjects increasing existing narcotics by 25%.
- Oral intakeUp to 6 weeks after radiation therapy
The number of subjects transitioning from solid to liquid or liquid to no oral intake.