Randomized Trial of Percutaneous vs. Endoscopic Gallbladder Drainage (PEG)
Percutaneous or Endoscopic Gallbladder Drainage: The PEG Trial
Visão geral do estudo
Status
Status
Condições
Condições
Intervenção / Tratamento
Intervenção / Tratamento
Descrição detalhada
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 de estudo
Tipo de estudo
Inscrição (Estimado)
Inscrição
Estágio
Estágio
- Não aplicável
Contactos e Locais
Contato de estudo
Contato de estudo
- Nome: Barbara J Broome
- Número de telefone: 321-841-4356
- E-mail: barbara.broome@orlandohealth.com
Estude backup de contato
- Nome: Ji Young Bang, MD MPH
- Número de telefone: 321-842-2273
- E-mail: jiyoung.bang@orlandohealth.com
Locais de estudo
-
-
Florida
-
Orlando, Florida, Estados Unidos, 32806
- Recrutamento
- Orlando Health Digestive Health Institute
-
Contato:
- Barbara J Broome
- Número de telefone: 321-841-4356
- E-mail: barbara.broome@orlandohealth.com
-
Contato:
- Ji Young Bang, MD MPH
- Número de telefone: 321-842-2273
- E-mail: jiyoung.bang@orlandohealth.com
-
-
Critérios de participação
Critérios de elegibilidade
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Número de braços
Armas e Intervenções
Grupo de Participantes / BraçoGrupo de Participantes / Braço |
Intervenção / TratamentoIntervenção / Tratamento |
|---|---|
|
Comparador Ativo: Percutaneous cholecystostomy
Patients with acute calculous cholecystitis who are never-surgery candidates undergoing percutaneous cholecystostomy tube placement
|
Percutaneous cholecystostomy tube placement by interventional radiology
|
|
Comparador Ativo: 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
|
O que o estudo está medindo?
Medidas de resultados primários
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
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
Prazo: 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
|
Medidas de resultados secundários
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Mortality
Prazo: 30 days
|
Rate of mortality at 30 days post-index intervention due to underlying disease.
|
30 days
|
|
Procedure-related adverse events
Prazo: 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
Prazo: 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.
Prazo: 36 months
|
Rate of new onset single and multiple organ failure.
|
36 months
|
|
New onset systemic dysfunction.
Prazo: 36 months
|
Rate of new onset systemic dysfunction.
|
36 months
|
|
Intraabdominal bleeding.
Prazo: 36 months
|
Rate of intraabdominal bleeding.
|
36 months
|
|
Leakage of bile from the gallbladder or the biliary tract.
Prazo: 36 months
|
Rate of leakage of bile from the gallbladder or the biliary tract.
|
36 months
|
|
Perforation of a visceral organ requiring interventional procedure.
Prazo: 36 months
|
Rate of perforation of a visceral organ requiring interventional procedure.
|
36 months
|
|
Stent or percutaneous catheter-related complications
Prazo: 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
Prazo: 36 months
|
Rate of disease recurrence, which includes acute cholecystitis or biliary colic.
|
36 months
|
|
Need for reintervention
Prazo: 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
Prazo: 36 months
|
Total number of reinterventions performed, including endoscopic, surgical and radiological interventions.
|
36 months
|
|
Length of hospitalization
Prazo: 36 months
|
Length of hospitalization, including length of ICU stay.
|
36 months
|
|
Readmissions
Prazo: 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.
Prazo: 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.
Prazo: 72 hours
|
Rate of Resolution and improvement of SIRS at 24, 48 and 72 hours, post-index intervention.
|
72 hours
|
|
Technical success
Prazo: 36 months
|
Rate of Technical success, defined as the successful placement of metal stent or percutaneous catheter.
|
36 months
|
|
Clinical success
Prazo: 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
Prazo: 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.
Prazo: 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
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Investigador principal: Ji Young Bang, MD MPH, Orlando Health, Digestive Health Institute
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Início do estudo
Conclusão Primária (Estimado)
Conclusão Primária
Conclusão do estudo (Estimado)
Conclusão do estudo
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Primeira postagem
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última Atualização Postada
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
Outros números de identificação do estudo
- 2440657
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .