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NCT06553651 · ClinicalTrials.gov registry record · NA
Necrosectomy With Cryotechnology for Accelerated Removal
A NA study of Acute Pancreatitis and Pancreatic Necrosis, sponsored by Christopher C. Thompson, MD, MSc.
- Recruiting
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT06553651: Recruiting NA study of Acute Pancreatitis and Pancreatic Necrosis, sponsored by Christopher C. Thompson, MD, MSc.
NCT06553651 is a NA study of Acute Pancreatitis and Pancreatic Necrosis that is actively recruiting participants, run by Christopher C. Thompson, MD, MSc. The registered enrollment target is 20 participants, below the 2,317-participant average among 10 other Acute Pancreatitis trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06553651, a NA study of Acute Pancreatitis and Pancreatic Necrosis, is actively recruiting participants, sponsored by Christopher C. Thompson, MD, MSc.
- RECRUITING
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
Pancreatic necrosis is a serious complication of acute pancreatitis. Pancreatic necrosis involves the irreversible death of pancreatic tissue, which can lead to severe health issues, including infections and an increased risk of death. An endoscopic procedure called direct endoscopic necrosectomy (DEN) is typically performed to remove this necrotic pancreatic tissue as a minimally invasive treatment. This procedure is performed using a thin, flexible, lighted tube called an endoscope and endoscopic instruments that are used with working channels through the scope. Current methods for removing necrotic tissue involve using endoscopic devices such as snares, baskets, nets, and forceps. However, these standard methods are often not very effective because the necrotic tissue can be sticky and hard to grasp. This DEN procedure is part of regular clinical care to treat this condition and remove necrotic tissue from the pancreas. For this research study, the same DEN procedure will be followed with the exception of the device used for the removal of the necrotic tissue. Instead of using forceps, snares, or other traditional tools, a cryoprobe will be used. Cryoprobes work by using extremely cold temperatures to freeze and adhere to the necrotic tissue, making it easier to remove. This method might be better because it can secure larger tissue samples and potentially reduce complications associated with traditional methods. Cryotechnology is successfully used in endoscopy to remove necrotic tissue, foreign bodies and more, but has not been extensively tested in pancreatic necrosis. Cryoprobes are FDA approved medical devices with an established safety record. They are used successfully in very sensitive areas such as the lungs. This study aims to evaluate the safety and effectiveness of cryotechnology for DEN.
Primary Outcome
To evaluate the effectiveness of cryotechnology for the removal of necrotic pancreatic tissue. Achievement of at least 70% removal of necrotic debris from the pancreatic collection being treated, as determined by change in computed tomography (CT) evaluation from baseline to 21 days post-treatment.
Conditions Studied
Interventions
- DEVICE Cryotechnology Necrosectomy Procedure
Study Locations (1)
Massachusetts
- Brigham and Women's Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2026-04 |
| Est. Completion | 2027-12 |
| Phase | NA |
What NCT06553651 shows while recruiting
NCT06553651 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 2,317-participant average among 10 other Acute Pancreatitis trials with a reported enrollment target (99% lower).
The record links to 6 conditions, with Acute Pancreatitis appearing as the primary indexed condition, and to 1 intervention - of which Cryotechnology Necrosectomy Procedure is the first listed.
NCT06553651 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT06553651 about?
NCT06553651 is a clinical study titled "Necrosectomy With Cryotechnology for Accelerated Removal". Pancreatic necrosis is a serious complication of acute pancreatitis. Pancreatic necrosis involves the irreversible death of pancreatic tissue, which can lead to severe health issues, including infections and an increased risk of death. An endoscopic procedure called direct endoscopic necrosectomy (D...
What is the current status of trial NCT06553651?
This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2026-04. Estimated completion is 2027-12.
What conditions does trial NCT06553651 study?
This clinical trial studies the following conditions: Acute Pancreatitis, Pancreatic Necrosis, Necrosis Pancreas, Acute Pancreatic Necrosis, Necrosis.
What interventions are being tested in trial NCT06553651?
The interventions under investigation include: Cryotechnology Necrosectomy Procedure (DEVICE).
Who is sponsoring clinical trial NCT06553651?
This trial is sponsored by Christopher C. Thompson, MD, MSc, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06553651 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT06553651's enrollment target sits among peer trials
20 11th of 10 the lowest of 10 other Acute Pancreatitis trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Acute Pancreatitis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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