Safety and Efficiency of Electrocautery-enhanced Lumen-apposing Stents - a Single Center Experience

Sponsor
Salzburger Landeskliniken (Other)
Overall Status
Recruiting
CT.gov ID
NCT05210842
Collaborator
(none)
200
1

Study Details

Study Description

Brief Summary

Lumen approximating stents have been used in interventional endoscopy to treat retentions in the upper gastrointestinal tract for 10 years. In the last few years, these have also been used with great success to form new anastomoses, especially in palliative patients. In this regard, many studies have been conducted in recent years.

As one of the largest centers for interventional endoscopy in Austria, we have been performing such interventions as standard since 2016.

The use of LAMS has become the standard therapy in many places. Most of the literature describes the technical advantages of LAMS, while the complications are less discussed. Although complications are rare with reported rates below 10%, with the multitude of technological and clinical advances in the field, it is important to understand and manage potential complications such as bleeding, perforation and stent migration.

Our goal is to evaluate the safety, efficacy, and outcome of all EC-LAMS in a single, high-volume center.

Method:

Suitable patients are analyzed retrospectively from the existing database. All patients who had a lumen-proximating stent implanted are included.

Condition or Disease Intervention/Treatment Phase
  • Other: Endoscopy

Detailed Description

Electrocautery-enhanced lumen-apposing stents (EC-LAMS) were originally designed for drainage of the gallbladder, bile duct, and pancreas pseudocysts.

Numerous studies have shown the effectiveness in treating pseudocysts, abscesses and walled-off pancreatic necrosis by creating a cystogastrostomy or cystoenterostomy tract with a LAMS for drainage and necrosectomy.

In patients suffering from acute cholecystitis, unfit for surgery due to significant comorbidities and/or essential need of anticoagulation, percutaneous gallbladder drainage (PTGBD) was considered as the viable treatment option. However, this procedure comes along with a high incidence of complications like bile leak, bowel perforation, catheter displacement, and cholangitis. Several studies compared the outcome of PTGBD with the endoscopic ultrasound-guided gallbladder drainage (EUS-GBD). The results show significantly superior results in the treatment of non-surgical acute cholecystitis patients with EUS-GBD, in order to consider the use of EUS-GBD as the treatment of choice.

Further, newer "off-label indications" of LAMS are to drain the bile duct in case of failed ERCP (endoscopic retrograde cholangiopancreatography) or, in patients where an ERCP is not possible due to malignant distal biliary obstructions, duodenal obstruction, or post-surgery anatomy. The creation of gastro-gastrostomy was used in patients with a gastric bypass to enable to perform an ERCP or drain a postoperative abscess/fluid collection. Results of published studies have already shown satisfactory clinical outcomes in stenting benign structures, mainly strictures near gastrointestinal (GI) anastomoses or due to chronic inflammations (gastroesophageal junction, pylorus).

We aim to evaluate the safety, efficacy, and outcome of all EC-LAMS placed in a single high-volume center.

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Safety and Efficiency of Electrocautery-enhanced Lumen-apposing Stents - a Single Center Experience
Anticipated Study Start Date :
Feb 1, 2022
Anticipated Primary Completion Date :
Feb 1, 2022
Anticipated Study Completion Date :
Feb 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Lumen apposing metal stent

All patients who had a lumen-proximating stent implanted are included.

Other: Endoscopy
The procedures are performed using a flexible therapeutic linear array echoendoscope.

Outcome Measures

Primary Outcome Measures

  1. Complications [2016-2021]

    The main outcome measure ist to evaluate how many complications occured during the use of lumen apposing metal stents in a single center

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18 - 99

  • Use of an electocautery-assisted lumen apposing stent

  • Follow-up of these patients for at least 3 months

Exclusion Criteria:
  • Age younger than 18

  • No use of an electrocautery-protected lumen-apposing stent

  • Lack of follow-up of at least 3 months

Contacts and Locations

Locations

Site City State Country Postal Code
1 Salzburger Landeskliniken Salzburg Austria 5020

Sponsors and Collaborators

  • Salzburger Landeskliniken

Investigators

  • Principal Investigator: Franz Singhartinger, Dr., Salzburger Landeskliniken

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Antonia Gantschnigg, Principal Investigator, Salzburger Landeskliniken
ClinicalTrials.gov Identifier:
NCT05210842
Other Study ID Numbers:
  • HA Salzburg
First Posted:
Jan 27, 2022
Last Update Posted:
Feb 10, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Antonia Gantschnigg, Principal Investigator, Salzburger Landeskliniken

Study Results

No Results Posted as of Feb 10, 2022