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

Description

To determine the safety and efficacy of GIE Medical's ProTractX3™ TTS DCB for the treatment of recurrent benign bowel strictures.

Conditions

Bowel; Stricture

Study Overview

Study Details

Study overview

To determine the safety and efficacy of GIE Medical's ProTractX3™ TTS DCB for the treatment of recurrent benign bowel strictures.

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

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

Condition
Bowel; Stricture
Intervention / Treatment

-

Contacts and Locations

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

Louisville

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

Marrero

Tandem Clinical Research, Marrero, Louisiana, United States, 70072

Brooklyn

New York Scientific, Brooklyn, New York, United States, 11235

New York

New York Presbyterian Hospital- Columbia University Medical Center, New York, New York, United States, 10027

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
  • 2. Diagnosis of symptomatic benign bowel stricture with at least 2 previous dilations.
  • 3. Willing and able to complete protocol required follow up
  • 4. Willing and able to provide written informed consent
  • 5. Stricture length ≤ 5 cm
  • 1. Female subjects who are pregnant or breastfeeding or plan to get pregnant in next 12 months
  • 2. Contraindication to endoscopy, anesthesia, or deep sedation.
  • 3. Suspicion of malignant bowel stricture NOTE: Biopsy should be taken for every stricture during the initial endoscopy, however endoscopic balloon dilation may proceed without awaiting results if suspicion for malignancy is low in the opinion of the investigator.
  • 4. Benign stricture due to extrinsic compression
  • 5. Stricture is not amenable to standard balloon dilation (e.g. severe angulation, unable to pass guidewire, etc.)
  • 6. Stricture complicated with abscess, fistula, perforation, leakage or varices
  • 7. Stricture segment has moderate to severe active inflammation at the time of treatment. Moderate to severe inflammation is defined as any one of; ulcers \>0.5cm in diameter, ulcerated surface \>10%, affected (inflamed) surface \>50%, marked erythema, absent vascular pattern, significant friability, or erosions
  • 8. Multiple clinically significant strictures unable to be treated with a single balloon (i.e. total segment length must be ≤5cm) NOTE: Clinically significant strictures include those that are unable to be passed by the endoscope.
  • 9. Received steroid injections into target stricture in the last 8 weeks
  • 10. Stricture is not able to be dilated to ≥15mm in small bowel or ≥18mm in large bowel
  • 11. Diagnosis of metastatic cancer of any type that is not considered in remission or non-metastatic cancer that may require radiation treatment in the pelvic region (e.g. prostate cancer)
  • 12. Suspected perforation of gastrointestinal tract
  • 13. Active systemic infection
  • 14. Allergy to paclitaxel
  • 15. Severe coagulation disorders or current use of anticoagulant or antiplatelet medication that cannot be safely managed per relevant societal guidelines
  • 16. Chronic systemic steroid use (defined as greater than 10 mg/day) for any medical conditions unless subject is willing to undergo a 4-week washout and discontinue steroid use
  • 17. Condition requiring treatment in urgent setting
  • 18. Life expectancy of less than 24 months
  • 19. 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, etc.
  • 20. Current participation in another pre-market drug or medical device clinical study unless in long term follow-up

Ages Eligible for Study

22 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

GIE Medical,

Study Record Dates

2029-03-01