Paclitaxel Coated Balloon for the Treatment of Chronic bEnigN sTricture- Esophagus

Description

To evaluate the safety and efficacy of the ProTractX3™ DCB for the treatment of benign esophageal strictures.

Conditions

Esophageal Stricture

Study Overview

Study Details

Study overview

To evaluate the safety and efficacy of the ProTractX3™ DCB for the treatment of benign esophageal strictures.

Paclitaxel Coated Balloon for the Treatment of Chronic bEnigN sTricture- Esophagus

Paclitaxel Coated Balloon for the Treatment of Chronic bEnigN sTricture- Esophagus

Condition
Esophageal Stricture
Intervention / Treatment

-

Contacts and Locations

Birmingham

Birmingham Gastroenterology Associates, Birmingham, Alabama, United States, 35209

North Little Rock

Arkansas Gastroenterology, North Little Rock, Arkansas, United States, 72117

Aurora

University of Colorado Anschutz, Aurora, Colorado, United States, 80045

Colorado Springs

Peak Gastroenterology, Colorado Springs, Colorado, United States, 80907

Gainesville

University of Florida, Gainesville, Florida, United States, 32610

Jacksonville

Borland-Groover, Jacksonville, Florida, United States, 32256

Orlando

Orlando Health, Orlando, Florida, United States, 32806

Macon

Gastroenterology Associates of Central Georgia, LLC, Macon, Georgia, United States, 31210

Chicago

Rush University, Chicago, Illinois, United States, 60612

Louisville

University of Louisville, Louisville, Kentucky, United States, 40202

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Age ≥ 22 years
  • 2. Diagnosis of a benign esophageal stricture with at least 2 previous dilations, at least one of which occurred in the last 12 months and achieved a diameter of 15mm
  • 3. Ogilvie Dysphagia Score of ≥2
  • 4. Minimum esophageal lumen diameter \<13 mm
  • 5. Willing and able to complete protocol required follow-up visits
  • 6. Willing and able to provide written informed consent
  • 7. Strictures ≤5cm in total length
  • 8. Target benign esophageal stricture etiologies include:
  • 1. Peptic stricture,
  • 2. Schatzki's ring,
  • 3. Stricture due to prior infection,
  • 4. Post-procedural (e.g. ESD/EMR/RFA/Cryo) stricture
  • 5. Post surgical (e.g. anastomotic), including post curative esophagectomy with or without prior neoadjuvant chemoradiation therapy
  • 1. Two or more clinically significant (e.g. non-traversable) strictures with total length \>5cm or unable to be treated with a single balloon.
  • 2. Female subjects who are pregnant or breastfeeding or plan to become pregnant in next 12 months
  • 3. Contraindication to endoscopy, anesthesia or deep sedation
  • 4. Benign esophageal stricture due to extrinsic esophageal compression, caustic ingestion, lichen planus, and purely radiation induced strictures (e.g. post head/neck cancer treatment).
  • 5. History of diagnosis of eosinophilic esophagitis (EoE)
  • 6. Signs or suspicion of a malignant esophageal stricture NOTE: If stricture is suspicious for malignancy based on clinical or endoscopic presentation, malignancy must be excluded by biopsy prior to enrollment. Subjects with a history of invasive esophageal cancer should have recurrence excluded by advanced imaging (e.g. CT/PET scan) and biopsy within 6 months of enrollment.
  • 7. Diagnosis of metastatic cancer of any type that is not considered in remission or non-metastatic cancer that may require radiation treatment in the neck or thoracic region NOTE: A prior diagnosis of esophageal cancer is acceptable if considered in remission and recurrence has been excluded by advanced imaging and biopsy within 6 months of enrollment.
  • 8. Suspected perforation of gastrointestinal tract
  • 9. Inability to pass guidewire across stricture
  • 10. Active systemic infection
  • 11. Allergy to paclitaxel or structurally related compounds
  • 12. Severe coagulation disorders or current use of anticoagulant or antiplatelet medication that cannot be safely managed per recommended guidelines prior to the index procedure
  • 13. Chronic systemic steroid use for any medical conditions unless subject is willing to undergo a 4-week washout and discontinue steroid use
  • 14. Received steroid injections into target stricture in the last 8 weeks.
  • 15. Stricture not amenable to endoscopic dilation to ≥ 18 mm in the opinion of the investigator
  • 16. Current use of feeding tube unless tube is removed prior to baseline assessments and subject maintains normal swallowing function.
  • 17. Acute stricture condition that requires emergent procedure (e.g. immediate dilation)
  • 18. Stricture complicated with abscess, fistula, deep ulceration, perforation, leakage or varices, or thrombosis, etc
  • 19. Life expectancy of less than 24 months
  • 20. Concurrent medical condition that would affect the investigator's ability to evaluate the patient's condition or could compromise patient safety, such as recent myocardial infarction, severe pulmonary disease, bleeding diathesis, large thoracic aneurysm, pharyngeal or cervical deformity, ongoing infection, etc
  • 21. Current participation in another pre-market drug or medical device clinical study that has not reached it's primary endpoint.
  • 22. Dysphagia related to primary motility disorders, such as achalasia, diffused esophageal spasm, ineffective esophageal motility (IEM), hypertensive lower esophageal sphincter, esophageal outlet obstruction, etc.
  • 23. Active erosive esophagitis with a Los Angeles classification of Grade B-D at the time of endoscopy.
  • 24. Significant esophageal dilation proximal to the stricture that, in the Investigator's opinion, may impact long-term esophageal motility.
  • 25. Intolerant to effective acid suppression medication (e.g. proton pump inhibitors, H2 receptor antagonists)
  • 26. Concurrent gastric and/or duodenal obstruction

Ages Eligible for Study

22 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

GIE Medical,

Study Record Dates

2029-12-01