Accelerated Marginal Ulcer Healing With Low-Thermal Argon Plasma Endoscopic Treatment

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The objective of the study is to investigate the treatment of marginal ulcers with Low Thermal plasma in an endoscopic setting. By a treatment of the ulcerated areas with argon plasma with low power settings (\ 1 W) we hypothesize that the size of the ulcers will shrink, and the healing is accelerated compared to standard of care alone. Patients will benefit from this minimally invasive approach compared to a much more invasive surgical approach that comes with higher risks and hospital stay length time. From a societal and scientific perspective, this study aims to extend the well-documented clinical benefits of plasma technology - from external wound healing to internal ulcer treatment - within an endoscopic framework. The success of this study could pave the way for broader applications of LTP in the treatment of other endoscopically accessible conditions such as peptic ulcers, duodenal ulcers and esophageal ulcers. This advancement has the potential not only to improve patient outcomes through less invasive methods, but also to position LTP as a cornerstone in the future of gastroenterological wound management strategies.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Subjects aged 18 years and above, inclusive of both males and females.

• Patients with a history of Roux-en-Y gastric bypass (RYGB) presenting symptoms indicative of marginal ulcers (MUs) such as abdominal pain, nausea, vomiting, gastrointestinal bleeding, or dysphagia.

• Subjects must be scheduled for an EGD for the evaluation of these symptoms.

• Marginal ulcers confirmed during the initial EGD.

• Willingness to adhere to the SOC treatment, which includes PPIs.

• Subjects able to tolerate repeated endoscopic procedures.

• Capacity for providing informed consent and understanding of study requirements.

• Willingness and ability to attend required follow-up assessments at 4 weeks (+/- 1 week) and 8 weeks (+/- 2 weeks).

Locations
United States
Massachusetts
Brigham and Women's Hospital
RECRUITING
Boston
Contact Information
Primary
Michele B Ryan, MS
mryan@bwh.harvard.edu
617-525-8266
Backup
Samantha Geltz
sgeltz@bwh.harvard.edu
617-732-5174
Time Frame
Start Date: 2025-03-04
Estimated Completion Date: 2027-04-30
Participants
Target number of participants: 100
Treatments
Active_comparator: Low Thermal Plasma (LTP)
Patients randomized to this group will receive LTP treatment of the ulcer in addition to SOC (PPI administration).
Active_comparator: Standard of Care (SOC) PPI Administration
Patients randomized to this group will receive only the SOC treatment (PPI administration).
Related Therapeutic Areas
Sponsors
Collaborators: Erbe USA Incorporated
Leads: Christopher C. Thompson, MD, MSc

This content was sourced from clinicaltrials.gov