BridgeMD
New treatment option for Stent Migration
Official title Anti-Migration System for Anti-reflux Oeso-gastric Stent (ANTIMIG)
ClinicalTrials.gov ID: NCT05431738
What this study is testing
- What it's testing
- The aim of this prospective, controlled, randomized, multicentre, single-blind study is to compare the rate of intragastric migration of 2 types of esophageal stents with and without an anti-migration device placed for locally advanced or metastatic malignant stenosis of the gastroesophageal junction.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 91
You may be able to join if
- Patient of both sexes aged 18 or over.
- Patient admitted to one of the investigation centers for dysphagia due to tumoral stenosis of the gastroesophageal junction, locally advanced or...
- Patient ASA 1, ASA 2, ASA 3
- Absence of participation in another clinical study
- Signed Informed Consent
You likely can't join if
- Patient referred for stenosis by extrinsic compression by an extra digestive mass
- Patients with contraindications relating to the procedures essential for the introduction of a stent
- Mediastinal radiotherapy or esophageal surgery history
- Patient under 18 or over 90
- Patient ASA 4, ASA 5
- Pregnant Woman
See the full eligibility criteria
- Patient of both sexes aged 18 or over.
- Patient admitted to one of the investigation centers for dysphagia due to tumoral stenosis of the gastroesophageal junction, locally advanced or metastatic.
- Patient ASA 1, ASA 2, ASA 3
- Absence of participation in another clinical study
- Signed Informed Consent
- Patients benefiting from the social security system.
- Patient referred for stenosis by extrinsic compression by an extra digestive mass
- Patients with contraindications relating to the procedures essential for the introduction of a stent
- Mediastinal radiotherapy or esophageal surgery history
- Patient under 18 or over 90
- Patient ASA 4, ASA 5
- Pregnant Woman
- Patient unable to give personal consent
- Absence of signed informed consent
The study team makes the final eligibility decision.
Where it's taking place
- Paris, France
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 91 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Paris, France. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.