Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Randomized Trial of Percutaneous vs. Endoscopic Gallbladder Drainage (PEG)

6 luglio 2026 aggiornato da: Orlando Health, Inc.

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.

Panoramica dello studio

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

110

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: Percutaneous cholecystostomy
Patients with acute calculous cholecystitis who are never-surgery candidates undergoing percutaneous cholecystostomy tube placement
Percutaneous cholecystostomy tube placement by interventional radiology
Comparatore attivo: EUS-guided gallbladder drainage
Patients with acute calculous cholecystitis who are never-surgery candidates, undergoing EUS-guided gallbladder drainage
EUS-guided gallbladder drainage using metal stent

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
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
Lasso di tempo: 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.
36 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Mortality
Lasso di tempo: 30 days
Rate of mortality at 30 days post-index intervention due to underlying disease.
30 days
Procedure-related adverse events
Lasso di tempo: 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.
36 months
Disease-related adverse events
Lasso di tempo: 36 months
Rate of disease-related adverse events, defined as adverse events resulting from underlying acute cholecystitis (such as gallbladder perforation, sepsis).
36 months
New onset single and multiple organ failure.
Lasso di tempo: 36 months
Rate of new onset single and multiple organ failure.
36 months
New onset systemic dysfunction.
Lasso di tempo: 36 months
Rate of new onset systemic dysfunction.
36 months
Intraabdominal bleeding.
Lasso di tempo: 36 months
Rate of intraabdominal bleeding.
36 months
Leakage of bile from the gallbladder or the biliary tract.
Lasso di tempo: 36 months
Rate of leakage of bile from the gallbladder or the biliary tract.
36 months
Perforation of a visceral organ requiring interventional procedure.
Lasso di tempo: 36 months
Rate of perforation of a visceral organ requiring interventional procedure.
36 months
Stent or percutaneous catheter-related complications
Lasso di tempo: 36 months
Rate of stent or percutaneous catheter-related complications, such as percutaneous catheter (cholecystostomy tube) insertion site infection, percutaneous catheter dislodgement.
36 months
Disease recurrence
Lasso di tempo: 36 months
Rate of disease recurrence, which includes acute cholecystitis or biliary colic.
36 months
Need for reintervention
Lasso di tempo: 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).
36 months
Total number of reinterventions performed
Lasso di tempo: 36 months
Total number of reinterventions performed, including endoscopic, surgical and radiological interventions.
36 months
Length of hospitalization
Lasso di tempo: 36 months
Length of hospitalization, including length of ICU stay.
36 months
Readmissions
Lasso di tempo: 36 months
Rate of readmissions due to symptoms from underlying disease or procedure-related adverse events.
36 months
New onset SIRS at 24, 48 and 72 hours, post-index intervention.
Lasso di tempo: 72 hours
Rate of New onset SIRS at 24, 48 and 72 hours, post-index intervention.
72 hours
Resolution and improvement of SIRS at 24, 48 and 72 hours, post-index intervention.
Lasso di tempo: 72 hours
Rate of Resolution and improvement of SIRS at 24, 48 and 72 hours, post-index intervention.
72 hours
Technical success
Lasso di tempo: 36 months
Rate of Technical success, defined as the successful placement of metal stent or percutaneous catheter.
36 months
Clinical success
Lasso di tempo: 36 months
Rate of Clinical success, defined as resolution of symptoms and normalization of laboratory parameters prior to hospital discharge after index intervention.
36 months
Health-related quality of life (HRQoL) scores
Lasso di tempo: 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.
36 months
Overall treatment costs from index intervention until hospital discharge.
Lasso di tempo: 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.
36 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Ji Young Bang, MD MPH, Orlando Health, Digestive Health Institute

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 luglio 2026

Completamento primario (Stimato)

1 giugno 2032

Completamento dello studio (Stimato)

1 dicembre 2032

Date di iscrizione allo studio

Primo inviato

6 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

6 luglio 2026

Primo Inserito (Effettivo)

10 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

10 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

6 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Colecistite acuta

Prove cliniche su Percutaneous cholecystostomy

3
Sottoscrivi