Skip to content

Self-Expandable Esophageal Radiation Stent:a Randomized Controlled Trial in Patients With Advanced Esophageal Cancer

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00477841
Enrollment
60
Registered
2007-05-24
Start date
2004-04-30
Completion date
2006-12-31
Last updated
2008-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Cancer

Keywords

esophageal Cancer, Dysphagia, Stent, interstitial brachytherapy

Brief summary

To determine the response to treatment with a novel esophageal stent loaded with 125I seeds for intraluminal brachytherapy versus a conventional covered stent in patients with advanced esophageal cancer.

Detailed description

Esophageal cancer is common in some areas , ranking as the fourth leading cause of death from cancer in China and sixth worldwide. Although the prognosis of surgical resection for esophageal cancer has been improved, more than 50% of such patients are inoperable and have to undergo palliative treatments because of late stage cancer or metastasis. Dysphagia is the predominate symptom of patients with inoperable esophageal cancer. To relieve the dysphagia and improve the quality of life of such patients, brachytherapy has previously been utilized. Recently, stent placement has been widely accepted to be an option for palliation of the symptoms due to the esophageal strictures. However, recurrence of the neoplastic stricture remains a challenge after stent placement. To combine the advantages of the immediate relief of the esophageal dysphagia with the stent placement and radiation therapy with brachytherapy, a novel esophageal stent loaded with 125I seeds has been developed in the authors' institute. The technical feasibility and safety with this new stent has been demonstrated to be adequate in a healthy rabbit model. The current study is designed to demonstrate the preliminary results with this irradiation stent in patients with inoperable esophageal cancer compared to those using a conventional covered stent.

Interventions

PROCEDUREdysphagia scores
PROCEDUREcomplications of therapy
PROCEDUREsurvival time of therapy

Sponsors

Southeast University, China
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Histologically confirmed primary cancer of esophagus, * Must be dysphagia caused by esophageal cancer, * Surgically inoperable, but may be metastatic, * Without esophageal fistulas, * Must be an inpatient at Zhongda Hospital, * Life expectancy is over 6 months,

Exclusion criteria

* Esophageal fistulas, * Tracheal compression with symptoms, * WBC \<2000/mm3 and Platelet count \<50,000/mm3, * Concurrent therapies:surgery, chemotherapy,radiotherapy, Traditional Chinese Medicine

Design outcomes

Primary

MeasureTime frame
Relief of dysphagia measured by dysphagia scores, survival time from the interventional procedure to the last follow-up.Follow-up in intervals of 1, 3, 6 and 12 months after stent placement

Secondary

MeasureTime frame
Successful rate of stent placement, Stent-related complications and morbidity, Overall rate of mortalityFollow-up in intervals of 1, 3, 6, and 12 months after stent placement

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026