Acute CholecystitisPEGNCT07696546
Randomized Trial of Percutaneous vs. Endoscopic Gallbladder Drainage
A study testing Percutaneous cholecystostomy and EUS-guided gallbladder drainage in people with Acute Cholecystitis, run by Orlando Health, Inc. at 1 site in United States.
Trial summary
This is a randomized trial of patients with acute calculous cholecystitis who are never-surgery candidates. Patients will be randomized to one of two treatment groups, percutaneous cholecystostomy or endoscopic ultrasound-guided drainage. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Acute Cholecystitis
- What is being tested?
- Percutaneous cholecystostomy and EUS-guided gallbladder drainage
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 110 participants
- Where
- 1 siteUnited States
- Study dates
- Jul 2026to Dec 2032
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients with suspected or confirmed acute calculous cholecystitis, diagnosed per Tokyo guidelines
- Age ≥ 18 years
- Patients due to severe comorbidity who are deemed to be never-surgery candidates by the multidisciplinary team or patients who refuse to undergo surgery.
- Patients can undergo EUS-guided drainage and percutaneous cholecystostomy tube placement.
- Written informed consent by the patient or guardian who can understand the nature and possible consequences of participation in the study.
Who cannot join
- Pregnancy
- Patients who are potential candidates for future cholecystectomy.
- Patients unwilling to undergo follow-up assessments.
- Patients with suspected gangrene or perforation of the gallbladder
- Patients are diagnosed with concomitant liver abscess or necrotizing pancreatitis.
- Altered anatomy of the upper gastrointestinal tract due to surgery of the esophagus, stomach and duodenum.
Show all 10Show fewer
- Indwelling percutaneous cholecystostomy tube.
- Refractory/persistently significant ascites despite paracentesis.
- Distance between the gallbladder and gastric/duodenal wall that cannot be bridged by the metal stent.
- Abnormal coagulation parameters that cannot be correct: INR > 1.7 and/or platelets < 50.000/mm3
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site, 1 recruiting
- Recruiting
Orlando Health Digestive Health Institute
Orlando, Florida, 32806
Ji Young Bang, MD MPH, 321-842-2273, jiyoung.bang@orlandohealth.com
Barbara J Broome, 321-841-4356, barbara.broome@orlandohealth.com
About this study
Official title: Percutaneous or Endoscopic Gallbladder Drainage: The PEG Trial
This is a randomized trial of patients with acute calculous cholecystitis who are never-surgery candidates. Patients will be randomized to one of two treatment groups, percutaneous cholecystostomy or endoscopic ultrasound-guided drainage. The aim of the study is to compare between these two treatment methods, the treatment outcomes and quality of life over a follow-up duration of 36 months.
Read the detailed description
Acute calculous cholecystitis (ACC) is characterized by an inflammatory condition involving the gallbladder wall, most often caused by an obstruction at the infundibulum or cystic duct, with less than 10% of cases provoked by other causes.
Surgical cholecystectomy (SC), especially by laparoscopic assistance, is considered the gold standard approach for the treatment of ACC. However, some patients due to high frailty, multiple comorbidities, and clinically significant organ failure are considered suboptimal or "unfit" candidates for surgery. Therefore, less invasive approaches have been developed for this challenging population.
Percutaneous choleystostomy (PC) has been traditionally considered the first alternative in patients who are not considered for surgery, as it is a less invasive approach with lower rates of complications compared to SC. The procedure is considered technically easy for experienced interventional radiologists and is based on the insertion of a percutaneous catheter in the gallbladder under fluoroscopic assistance after an ultrasound-guided puncture with an 18-gauge needle. Nevertheless, like any other procedure, PC is not exempt from complications, such as bleeding, pneumothorax, peritonitis, injury to adjacent organs, pain at the site of insertion, catheter dislodgement, and risk for recurrent cholecystitis upon removal of the catheter.
Endoscopic ultrasound (EUS)-guided gallbladder drainage (EUS-GBD) has been described as another minimally invasive option for these patients. Under endoscopic ultrasound-guidance, a lumen-apposing metal stent is placed within the gallbladder lumen from the stomach or the duodenum (EUS-GBD), thus allowing internal drainage. EUS-GBD appears to have some benefits over PC, since the latter is typically associated with patient's discomfort and pain at the site of insertion, and carries inherent disadvantages associated with external drainage.
The management of ACC in patients who are not surgical candidates is complex. These patients carry a high risk of peri-cholecystectomy and post-cholecystectomy complications and a mortality rate of up to 19%. The initial management of patients who are not surgical candidates consists of antibiotic therapy and minimally invasive procedures for adequate gallbladder drainage. These procedures include PC and endoscopy-guided gallbladder drainage. Tokyo Guidelines-2018 (TG-18) recommend PC as the standard drainage method for surgically high-risk patients with AC. World Society of Emergency Surgery 2020 guidelines recommend considering endoscopic transpapillary gallbladder drainage (ET-GBD) or EUS-GBD as an alternative to PC in high-volume centers when performed by skilled endoscopists. There is a lumen-apposing metal stent (LAMS), which was recently approved by the Food and Drug Administration (FDA) for EUS-GBD in poor surgical candidates.
In a prior study (DRAC 1) that compared PC versus EUS-GBD in high-risk patients with ACC, EUS-GBD was associated with significantly fewer adverse events, readmissions and recurrent cholecystitis. However, the follow-up duration was only 12 months, which is a very short timeframe to reliably compare long-term outcomes between modalities. This is particularly relevant as nearly 45% of patients who do not receive a cholecystectomy die within 825 days of an attack of ACC. Also, health-related quality of life and treatment costs were not assessed in DRAC 1. Finally, the primary outcome in the DRAC 1 trial was only a single measure - adverse events. The burden of ACC and the impact of treatment is more accurately measured using a composite endpoint encompassing readmissions and reinterventions in addition to adverse events.
We hypothesize that by performing EUS-GBD as the first-line therapy in never-surgery patients presenting with ACC, the rates of procedural reinterventions, readmissions, and disease or procedure-related adverse events can be reduced as compared to patents undergoing percutaneous cholecystostomy.
- Conditions
- Acute Cholecystitis
- Being tested
- Percutaneous cholecystostomy, EUS-guided gallbladder drainage
- Keywords
- EUS-guided gallbladder drainage, percutaneous cholecystostomy, Acute calculous cholecystitis, Endoscopic ultrasound, Interventional radiology
- Medical subject headings
- Cholecystitis, Acute
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Percutaneous cholecystostomyProcedure or surgery
Percutaneous cholecystostomy tube placement by interventional radiology
EUS-guided gallbladder drainageProcedure or surgery
EUS-guided gallbladder drainage using metal stent
| Study group | Role | What they receive |
|---|---|---|
| Percutaneous cholecystostomy | Active comparator | Patients with acute calculous cholecystitis who are never-surgery candidates undergoing percutaneous cholecystostomy tube placement Receives: Procedure: Percutaneous cholecystostomy |
| EUS-guided gallbladder drainage | Active comparator | Patients with acute calculous cholecystitis who are never-surgery candidates, undergoing EUS-guided gallbladder drainage Receives: Procedure: EUS-guided gallbladder drainage |
What is being measured
The primary outcome is the main question the study is designed to answer.
Composite endpoint of 1) procedure-related adverse events, 2) reintervention for disease recurrence or procedure-related adverse events, and/or 3) readmission due to underlying disease or procedure-related adverse events
A composite endpoint of 1) procedure-related adverse events, 2) reintervention for disease recurrence or procedure-related adverse events, and/or 3) readmission due to underlying disease or procedure-related adverse events, from index procedure to 36 months post-index intervention.
Measured: 36 months
Secondary outcomes (20)
Mortality
Rate of mortality at 30 days post-index intervention due to underlying disease.
Measured: 30 days
Procedure-related adverse events
Rate of procedure-related adverse events, defined as adverse events resulting from the endoscopic or radiological procedures performed. Procedure-related adverse events will be graded according to Clavien-Dindo classification.
Measured: 36 months
Disease-related adverse events
Rate of disease-related adverse events, defined as adverse events resulting from underlying acute cholecystitis (such as gallbladder perforation, sepsis).
Measured: 36 months
New onset single and multiple organ failure.
Rate of new onset single and multiple organ failure.
Measured: 36 months
New onset systemic dysfunction.
Rate of new onset systemic dysfunction.
Measured: 36 months
Intraabdominal bleeding.
Rate of intraabdominal bleeding.
Measured: 36 months
Leakage of bile from the gallbladder or the biliary tract.
Rate of leakage of bile from the gallbladder or the biliary tract.
Measured: 36 months
Perforation of a visceral organ requiring interventional procedure.
Rate of perforation of a visceral organ requiring interventional procedure.
Measured: 36 months
Stent or percutaneous catheter-related complications
Rate of stent or percutaneous catheter-related complications, such as percutaneous catheter (cholecystostomy tube) insertion site infection, percutaneous catheter dislodgement.
Measured: 36 months
Disease recurrence
Rate of disease recurrence, which includes acute cholecystitis or biliary colic.
Measured: 36 months
Need for reintervention
Rate of reintervention (reintervention defined as any unplanned endoscopic, radiological or surgical intervention performed following index intervention due to recurrent or persistent symptoms or acute cholecystitis).
Measured: 36 months
Total number of reinterventions performed
Total number of reinterventions performed, including endoscopic, surgical and radiological interventions.
Measured: 36 months
Length of hospitalization
Length of hospitalization, including length of ICU stay.
Measured: 36 months
Readmissions
Rate of readmissions due to symptoms from underlying disease or procedure-related adverse events.
Measured: 36 months
New onset SIRS at 24, 48 and 72 hours, post-index intervention.
Rate of New onset SIRS at 24, 48 and 72 hours, post-index intervention.
Measured: 72 hours
Resolution and improvement of SIRS at 24, 48 and 72 hours, post-index intervention.
Rate of Resolution and improvement of SIRS at 24, 48 and 72 hours, post-index intervention.
Measured: 72 hours
Technical success
Rate of Technical success, defined as the successful placement of metal stent or percutaneous catheter.
Measured: 36 months
Clinical success
Rate of Clinical success, defined as resolution of symptoms and normalization of laboratory parameters prior to hospital discharge after index intervention.
Measured: 36 months
Health-related quality of life (HRQoL) scores
Health-related quality of life (HRQoL) scores as assessed by the Medical Outcomes Study 36-Item Short-Form General Health Survey (SF-36) at randomization, discharge, 1 month, 3 months, 6 months, 12 months, 18 months, 24 months, 30 months and 36 months after index intervention.
Measured: 36 months
Overall treatment costs from index intervention until hospital discharge.
Overall treatment costs from index intervention until hospital discharge. All relevant costs pertaining to treatment will be taken into consideration - procedure costs, inpatient hospital stay from date of procedure to discharge, medications, materials, anesthesia, pharmacy and imaging studies.
Measured: 36 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Jul 2026
- Study startJul 2026 (estimated)
- Primary completionJun 2032 (estimated)
- Study completionDec 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Acute CholecystitisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 110 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Orlando Health, Inc.
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Ji Young Bang, MD MPH, Principal investigator, Orlando Health, Digestive Health Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07696546
- Sponsor's protocol ID
- 2440657
- Acronym
- PEG
- Status last verified
- Jul 2026
- First submitted
- 6 Jul 2026
- Last updated
- 10 Jul 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Percutaneous or Endoscopic Gallbladder Drainage: The PEG Trial
- ClinicalTrials.gov ID
- NCT07696546
- Acronym / sponsor ID
- PEG / 2440657
- Conditions
- Acute Cholecystitis
- Keywords
- EUS-guided gallbladder drainage, percutaneous cholecystostomy, Acute calculous cholecystitis, Endoscopic ultrasound, Interventional radiology
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 110 participants (estimated)
- Lead sponsor
- Orlando Health, Inc.University, hospital or other
- Study start
- Jul 2026 (estimated)
- Primary completion
- Jun 2032 (estimated)
- Study completion
- Dec 2032 (estimated)
- First posted
- 10 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a randomized trial of patients with acute calculous cholecystitis who are never-surgery candidates. Patients will be randomized to one of two treatment groups, percutaneous cholecystostomy or endoscopic ultrasound-guided drainage. The aim of the study is to compare between these two treatment methods, the treatment outcomes and quality of life over a follow-up duration of 36 months.
Detailed description
Acute calculous cholecystitis (ACC) is characterized by an inflammatory condition involving the gallbladder wall, most often caused by an obstruction at the infundibulum or cystic duct, with less than 10% of cases provoked by other causes.
Surgical cholecystectomy (SC), especially by laparoscopic assistance, is considered the gold standard approach for the treatment of ACC. However, some patients due to high frailty, multiple comorbidities, and clinically significant organ failure are considered suboptimal or "unfit" candidates for surgery. Therefore, less invasive approaches have been developed for this challenging population.
Percutaneous choleystostomy (PC) has been traditionally considered the first alternative in patients who are not considered for surgery, as it is a less invasive approach with lower rates of complications compared to SC. The procedure is considered technically easy for experienced interventional radiologists and is based on the insertion of a percutaneous catheter in the gallbladder under fluoroscopic assistance after an ultrasound-guided puncture with an 18-gauge needle. Nevertheless, like any other procedure, PC is not exempt from complications, such as bleeding, pneumothorax, peritonitis, injury to adjacent organs, pain at the site of insertion, catheter dislodgement, and risk for recurrent cholecystitis upon removal of the catheter.
Endoscopic ultrasound (EUS)-guided gallbladder drainage (EUS-GBD) has been described as another minimally invasive option for these patients. Under endoscopic ultrasound-guidance, a lumen-apposing metal stent is placed within the gallbladder lumen from the stomach or the duodenum (EUS-GBD), thus allowing internal drainage. EUS-GBD appears to have some benefits over PC, since the latter is typically associated with patient's discomfort and pain at the site of insertion, and carries inherent disadvantages associated with external drainage.
The management of ACC in patients who are not surgical candidates is complex. These patients carry a high risk of peri-cholecystectomy and post-cholecystectomy complications and a mortality rate of up to 19%. The initial management of patients who are not surgical candidates consists of antibiotic therapy and minimally invasive procedures for adequate gallbladder drainage. These procedures include PC and endoscopy-guided gallbladder drainage. Tokyo Guidelines-2018 (TG-18) recommend PC as the standard drainage method for surgically high-risk patients with AC. World Society of Emergency Surgery 2020 guidelines recommend considering endoscopic transpapillary gallbladder drainage (ET-GBD) or EUS-GBD as an alternative to PC in high-volume centers when performed by skilled endoscopists. There is a lumen-apposing metal stent (LAMS), which was recently approved by the Food and Drug Administration (FDA) for EUS-GBD in poor surgical candidates.
In a prior study (DRAC 1) that compared PC versus EUS-GBD in high-risk patients with ACC, EUS-GBD was associated with significantly fewer adverse events, readmissions and recurrent cholecystitis. However, the follow-up duration was only 12 months, which is a very short timeframe to reliably compare long-term outcomes between modalities. This is particularly relevant as nearly 45% of patients who do not receive a cholecystectomy die within 825 days of an attack of ACC. Also, health-related quality of life and treatment costs were not assessed in DRAC 1. Finally, the primary outcome in the DRAC 1 trial was only a single measure - adverse events. The burden of ACC and the impact of treatment is more accurately measured using a composite endpoint encompassing readmissions and reinterventions in addition to adverse events.
We hypothesize that by performing EUS-GBD as the first-line therapy in never-surgery patients presenting with ACC, the rates of procedural reinterventions, readmissions, and disease or procedure-related adverse events can be reduced as compared to patents undergoing percutaneous cholecystostomy.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Percutaneous cholecystostomy | Active comparator | Procedure: Percutaneous cholecystostomyPatients with acute calculous cholecystitis who are never-surgery candidates undergoing percutaneous cholecystostomy tube placement |
| EUS-guided gallbladder drainage | Active comparator | Procedure: EUS-guided gallbladder drainagePatients with acute calculous cholecystitis who are never-surgery candidates, undergoing EUS-guided gallbladder drainage |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Patients with suspected or confirmed acute calculous cholecystitis, diagnosed per Tokyo guidelines
- Age ≥ 18 years
- Patients due to severe comorbidity who are deemed to be never-surgery candidates by the multidisciplinary team or patients who refuse to undergo surgery.
- Patients can undergo EUS-guided drainage and percutaneous cholecystostomy tube placement.
- Written informed consent by the patient or guardian who can understand the nature and possible consequences of participation in the study.
Key exclusion criteria (10 listed)
- Pregnancy
- Patients who are potential candidates for future cholecystectomy.
- Patients unwilling to undergo follow-up assessments.
- Patients with suspected gangrene or perforation of the gallbladder
- Patients are diagnosed with concomitant liver abscess or necrotizing pancreatitis.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Percutaneous cholecystostomyPercutaneous cholecystostomy tube placement by interventional radiology | Procedure or surgery | Percutaneous cholecystostomy |
| EUS-guided gallbladder drainageEUS-guided gallbladder drainage using metal stent | Procedure or surgery | EUS-guided gallbladder drainage |
Primary outcome
Composite endpoint of 1) procedure-related adverse events, 2) reintervention for disease recurrence or procedure-related adverse events, and/or 3) readmission due to underlying disease or procedure-related adverse events
Time frame: 36 months
A composite endpoint of 1) procedure-related adverse events, 2) reintervention for disease recurrence or procedure-related adverse events, and/or 3) readmission due to underlying disease or procedure-related adverse events, from index procedure to 36 months post-index intervention.
20 secondary outcomes
Mortality
Time frame: 30 days
Procedure-related adverse events
Time frame: 36 months
Disease-related adverse events
Time frame: 36 months
New onset single and multiple organ failure.
Time frame: 36 months
New onset systemic dysfunction.
Time frame: 36 months
Intraabdominal bleeding.
Time frame: 36 months
Leakage of bile from the gallbladder or the biliary tract.
Time frame: 36 months
Perforation of a visceral organ requiring interventional procedure.
Time frame: 36 months
Stent or percutaneous catheter-related complications
Time frame: 36 months
Disease recurrence
Time frame: 36 months
Need for reintervention
Time frame: 36 months
Total number of reinterventions performed
Time frame: 36 months
Length of hospitalization
Time frame: 36 months
Readmissions
Time frame: 36 months
New onset SIRS at 24, 48 and 72 hours, post-index intervention.
Time frame: 72 hours
Resolution and improvement of SIRS at 24, 48 and 72 hours, post-index intervention.
Time frame: 72 hours
Technical success
Time frame: 36 months
Clinical success
Time frame: 36 months
Health-related quality of life (HRQoL) scores
Time frame: 36 months
Overall treatment costs from index intervention until hospital discharge.
Time frame: 36 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jul 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Ji Young Bang, MD MPH principal investigator
Orlando Health, Digestive Health Institute
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Percutaneous cholecystostomy and EUS-guided gallbladder drainage in people with Acute Cholecystitis, run by Orlando Health, Inc. at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 10 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Ji Young Bang, MD MPH (321-842-2273, jiyoung.bang@orlandohealth.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Composite endpoint of 1) procedure-related adverse events, 2) reintervention for disease recurrence or procedure-related adverse events, and/or 3) readmission due to underlying disease or procedure-related adverse events (time frame: 36 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jul 2026.