Role of Home-based Transcutaneous Electrical Acustimulation for Treatment of Pain in Patients With Chronic Pancreatitis
Completed · Not applicable
Conditions studied: Chronic Pancreatitis
In brief
This research is studying a new noninvasive device-based therapy called Transcutaneous Electrical Acustimulation (TEA) to learn about its safety and how well it works as a treatment of pain in chronic pancreatitis. The purpose of this study is to investigate the potential of TEA to treat abdominal pain in patients with chronic pancreatitis (CP). The study hypothesizes that TEA can be used as a non-pharmaceutical opioid-free approach to treat pain in chronic pancreatitis.
Key facts
- Study ID
- NCT06015945
- Run by
- University of Michigan
- People needed
- 12
- Starts
- 2023-10-05
- Expected to finish
- 2024-12-01
- Last updated by the study team
- 2026-02-04
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of chronic pancreatitis (CP), based on a score greater or equal to 4 using a previously validated Mayo scoring system that uses morphologic and functional criteria, or endosonographic features suggestive or consistent with CP based on Rosemont criteria.
- Abdominal pain present at least once within the last month
- Willing and able to provide written informed consent
You may not qualify if…
- Pregnancy or breastfeeding mother
- Imprisoned individuals
- Non-English speaking patients
- Scheduled for or with a history of pancreatic surgery (e.g. Total Pancreatectomy with Islet Auto Transplantation (TPIAT), Puestow, Frey, Whipple, other)
- Currently undergoing or about to start endoscopic therapy with Endoscopic retrograde cholangiopancreatography (ERCP) or Endoscopic ultrasound (EUS)
- Recent history of acute pancreatitis as defined by the Revised Atlanta Classification within a month prior to enrollment
- Radiologic and clinical findings consistent with symptomatic pseudocyst, wall-off necrosis, infected pancreatic necrosis, or biliary obstruction within the last 6 months
- Self-reported daily use of opioids for > 12 months for weak opioids (codeine, tramadol and hydrocodone) or > 6 months for strong opioids (other opioids) in the last two years.
- Self-reported ongoing illicit drug use or abuse-
- Suspected or diagnosed pancreatic cancer
- Receiving chemotherapy for cancer
- Known allergy to adhesive electrocardiogram (ECG) electrodes
- Patients with bilateral below the knee amputation
- Patients with lower extremity paralysis
- Patient is participating in another clinical trial
- Patients with an implantable electrical stimulation device.
Where it is running
- University of Michigan — Ann Arbor, Michigan, United States
Full record on ClinicalTrials.gov
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