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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.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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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
  • 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

    Recruiting

Other trials in United States

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.

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 groups in NCT07696546
Study groupRoleWhat they receive
Percutaneous cholecystostomyActive comparatorPatients with acute calculous cholecystitis who are never-surgery candidates undergoing percutaneous cholecystostomy tube placement
Receives: Procedure: Percutaneous cholecystostomy
EUS-guided gallbladder drainageActive comparatorPatients 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.

  1. 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)
  1. Mortality

    Rate of mortality at 30 days post-index intervention due to underlying disease.

    Measured: 30 days

  2. 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

  3. 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

  4. New onset single and multiple organ failure.

    Rate of new onset single and multiple organ failure.

    Measured: 36 months

  5. New onset systemic dysfunction.

    Rate of new onset systemic dysfunction.

    Measured: 36 months

  6. Intraabdominal bleeding.

    Rate of intraabdominal bleeding.

    Measured: 36 months

  7. 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

  8. Perforation of a visceral organ requiring interventional procedure.

    Rate of perforation of a visceral organ requiring interventional procedure.

    Measured: 36 months

  9. 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

  10. Disease recurrence

    Rate of disease recurrence, which includes acute cholecystitis or biliary colic.

    Measured: 36 months

  11. 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

  12. Total number of reinterventions performed

    Total number of reinterventions performed, including endoscopic, surgical and radiological interventions.

    Measured: 36 months

  13. Length of hospitalization

    Length of hospitalization, including length of ICU stay.

    Measured: 36 months

  14. Readmissions

    Rate of readmissions due to symptoms from underlying disease or procedure-related adverse events.

    Measured: 36 months

  15. 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

  16. 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

  17. Technical success

    Rate of Technical success, defined as the successful placement of metal stent or percutaneous catheter.

    Measured: 36 months

  18. 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

  19. 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

  20. 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.

  1. First posted10 Jul 2026
  2. Study startJul 2026 (estimated)
  3. Primary completionJun 2032 (estimated)
  4. Study completionDec 2032 (estimated)

Resources

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)
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

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.

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