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NCT Number: NCT07696546

Randomized Trial of Percutaneous vs. Endoscopic Gallbladder Drainage

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.
  • 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

Treatment and study plan

PERCUTANEOUS CHOLECYSTOSTOMY

Procedure

Percutaneous cholecystostomy tube placement by interventional radiology

EUS-guided gallbladder drainage

Procedure

EUS-guided gallbladder drainage using metal stent

Primary outcomes

  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

    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.

Secondary outcomes

  1. Mortality

    Time frame: 30 days

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

  2. Procedure-related adverse events

    Time frame: 36 months

    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.

  3. Disease-related adverse events

    Time frame: 36 months

    Rate of disease-related adverse events, defined as adverse events resulting from underlying acute cholecystitis (such as gallbladder perforation, sepsis).

  4. New onset single and multiple organ failure.

    Time frame: 36 months

    Rate of new onset single and multiple organ failure.

  5. New onset systemic dysfunction.

    Time frame: 36 months

    Rate of new onset systemic dysfunction.

  6. Intraabdominal bleeding.

    Time frame: 36 months

    Rate of intraabdominal bleeding.

  7. Leakage of bile from the gallbladder or the biliary tract.

    Time frame: 36 months

    Rate of leakage of bile from the gallbladder or the biliary tract.

  8. Perforation of a visceral organ requiring interventional procedure.

    Time frame: 36 months

    Rate of perforation of a visceral organ requiring interventional procedure.

  9. Stent or percutaneous catheter-related complications

    Time frame: 36 months

    Rate of stent or percutaneous catheter-related complications, such as percutaneous catheter (cholecystostomy tube) insertion site infection, percutaneous catheter dislodgement.

  10. Disease recurrence

    Time frame: 36 months

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

  11. Need for reintervention

    Time frame: 36 months

    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).

  12. Total number of reinterventions performed

    Time frame: 36 months

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

  13. Length of hospitalization

    Time frame: 36 months

    Length of hospitalization, including length of ICU stay.

  14. Readmissions

    Time frame: 36 months

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

  15. New onset SIRS at 24, 48 and 72 hours, post-index intervention.

    Time frame: 72 hours

    Rate of New onset SIRS at 24, 48 and 72 hours, post-index intervention.

  16. Resolution and improvement of SIRS at 24, 48 and 72 hours, post-index intervention.

    Time frame: 72 hours

    Rate of Resolution and improvement of SIRS at 24, 48 and 72 hours, post-index intervention.

  17. Technical success

    Time frame: 36 months

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

  18. Clinical success

    Time frame: 36 months

    Rate of Clinical success, defined as resolution of symptoms and normalization of laboratory parameters prior to hospital discharge after index intervention.

  19. Health-related quality of life (HRQoL) scores

    Time frame: 36 months

    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.

  20. Overall treatment costs from index intervention until hospital discharge.

    Time frame: 36 months

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Barbara J Broome

CONTACT

[email protected]

321-841-4356

Ji Young Bang, MD MPH

CONTACT

[email protected]

321-842-2273

Sponsors and collaborators

Lead sponsor

Orlando Health, Inc.

Other

Registry information

Official study title

Percutaneous or Endoscopic Gallbladder Drainage: The PEG Trial

Acronym: PEG

Important dates

Study start
2026
Primary completion
2032
Study completion
2032
First posted
Jul 10, 2026
Registry last updated
Jul 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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