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Trial Title:
Management of Malignant Gastric Outlet Obstruction Between Surgery and Endoscopy
NCT ID:
NCT06071507
Condition:
Gastric Outlet Obstruction
Pancreatic Cancer
Conditions: Official terms:
Gastric Outlet Obstruction
Pyloric Stenosis
Conditions: Keywords:
Enteral stent
Duodenal stent
Gastroenterostomy
EUS
Bypass
LAMS
Gastrojejunostomy
Study type:
Observational [Patient Registry]
Overall status:
Recruiting
Study design:
Time perspective:
Prospective
Summary:
The aim of this observational study is to compare the outcomes of three different
procedures performed for the management of malignant Gastric Outlet Obstruction due to
Pancreatic Cancer.
Patients who undergo:
- Surgical gastroenterostomy
- Endoscopic placement of a self-expanding metallic stent
- EUS-guided gastroenterostomy in accordance with standard clinical practice, will be
enrolled to evaluate potential differences between the procedures in terms of
clinical success, eating experience, chemotherapy tolerance, and nutritional status
during follow-up.
Participants will be asked to complete a quality of life questionnaire at baseline and
during follow-up; however, no additional procedures will be conducted as a result of
participation in the study.
Detailed description:
Gastric Outlet Obstruction (GOO) syndrome is a frequent complication of biliopancreatic
and gastroduodenal neoplasms and manifests with recurrent vomiting, dehydration and
malnutrition, seriously compromising quality of life and the ability to tolerate
chemotherapy.
Standard treatment options for GOO are surgical gastroenterostomy (S-GE) or endoscopic
placement of a self-expanding metallic stent (ES): surgical treatment achieves better
long-term results at the cost of a more invasive procedure. The advances of therapeutic
endosonography (EUS) have provided a new possibility to resolve this condition through
EUS-guided gastroenterostomy (EUS-GE). The latter involves the creation of a
gastroenteric bypass by endoscopically positioning a lumen-apposing metal stent (LAMS).
Recent evidence has shown several advantages over previous treatments, in terms of less
invasiveness compared to surgery and greater long-term efficacy compared to enteral
stenting. However, most of the evidence comes from retrospective protocols and
heterogeneous studies that include different neoplasms and clinical courses. Furthermore,
the definition of clinical success in the current literature refers to the resolution of
the mechanical obstruction of the syndrome, without any in-depth study on the clinical
impact of different management strategies in terms of more complex outcomes, such as
survival, quality of life, nutritional status and chemotherapy tolerance.
The aim of this study is to prospectively analyze the long-term clinical impact of GOO
management strategies in a homogeneous cohort of patients with pancreatic adenocarcinoma
(PC) and recent disease diagnosis.
The design of this study is:
- Observational
- Prospective
- Multicentric
- Comparative (3-arms)
No changes to the current clinical practice of the participating centers are foreseen.
Each center will candidate the enrolled patient to the procedure that is routinely and
currently used in that clinical scenario at their own center. Enrollment in the protocol
does not require additional investigations or treatments, except for the administration
of quality-of-life questionnaires. Participation in the study implies sharing of
information standardly collected during the oncological journey. The prospective
follow-up will address clinical efficacy, safety and patient-reported experience,
including assessment of the eating experience, chemotherapy tolerance and nutritional
status.
Criteria for eligibility:
Study pop:
A homogeneous population of patients with pathologically confirmed Pancreatic Cancer,
candidate to palliation of Gastric Outlet Obstruction and active oncological treatment.
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
- cyto-/histo-logically confirmed pancreatic cancer
- a maximum of 6 months from pancreatic cancer diagnosis and candidate to active
treatment
- stenosis causing gastric outlet obstruction (GOO) due to neoplastic
invasion/compression confirmed by radiology or endoscopy extending from the distal
one third of the stomach or the duodenum
- patients candidate to either ES or EUS-GE or s-GE
Exclusion Criteria:
- age < 18 years
- patients with benign or indeterminate gastrointestinal stenosis
- patients with malignant GOO (mGOO) from neoplasia other than pancreatic cancer
- candidates to upfront surgical resection or who already received curative pancreatic
resection
- patients who already received a treatment for mGOO
- patients receiving an additional procedure for biliary drainage which might increase
the risk of adverse events or hamper the assessment of quality of life; biliary
drainage will be allowed if performed uneventfully (without adverse events) at least
one day (endoscopic drainage) or one month (surgical hepaticojejunostomy) before
mGOO treatment;
- patients carrying any percutaneous drainage (such as percutaneous transhepatic
biliary drainage or ascites drainage).
- inability or unwillingness to sign the informed consent form (ICF)
- contraindications to any active palliation of the mGOO, or indication to palliation
through venting gastrostomy or nasogastric tube placement alone
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Hôpital la pitié salpêtrière, APHP
Address:
City:
Paris
Country:
France
Status:
Not yet recruiting
Contact:
Last name:
Charles De Ponthaud
Contact backup:
Last name:
Sebastien Gaujoux
Facility:
Name:
IRCCS San Raffaele Scientific Institute
Address:
City:
Milan
Zip:
20132
Country:
Italy
Status:
Recruiting
Contact:
Last name:
Giuseppe Vanella, MD
Phone:
+390226439574
Email:
vanella.giuseppe@hsr.it
Facility:
Name:
ISMETT - University of Palermo
Address:
City:
Palermo
Country:
Italy
Status:
Not yet recruiting
Contact:
Last name:
Giacomo Rizzo
Facility:
Name:
São João University Hospital
Address:
City:
Porto
Country:
Portugal
Status:
Not yet recruiting
Contact:
Last name:
Filipe Vilas Boas Silva
Facility:
Name:
Acibadem Maslak Hospital
Address:
City:
Istanbul
Country:
Turkey
Status:
Not yet recruiting
Contact:
Last name:
Bahadir Bozkırlı
Start date:
April 15, 2024
Completion date:
December 2027
Lead sponsor:
Agency:
IRCCS San Raffaele
Agency class:
Other
Collaborator:
Agency:
European Pancreatic Club
Agency class:
Other
Collaborator:
Agency:
The Mediterranean Institute for Transplantation and Advanced Specialized Therapies
Agency class:
Other
Source:
IRCCS San Raffaele
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06071507