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Kaffes Stent in the Management of Post-surgical Biliary Strictures

The Safety and Efficacy of a Short Specially Designed Fully Covered Metallic Stent in the Management of Benign Post-surgical Biliary Strictures: a Randomized-controlled Study

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03716232
Enrollment
30
Registered
2018-10-23
Start date
2018-07-01
Completion date
2020-12-31
Last updated
2020-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign Biliary Stricture, Bile Duct Injury, Bile Duct Stricture, Biliary Stricture, Cholangitis

Brief summary

Post-surgical biliary strictures are common especially after cholecystectomy. Standard treatment involves the performance of multiple procedures over a 1 year period at least using several plastic stents to achieve permanent dilatation of these strictures. Metallic stents have the theoretical benefit of absence of need of multiple sessions. These strictures however are frequently very close to the hilum and thus previously considered a contraindication for insertion of metallic stents for the fear of occlusion of the contralateral ducts. Metallic stent migration is also a frequent problem. The use of a metallic stent that is short and completely intraductal, in theory, should reduce the risk of stent migration. This is a randomized controlled trial comparing the efficacy and safety of a short metallic intraductal stent to the conventional treatment which is multiple plastic stents. In cases with a stricture reaching or close to the hilum a technique is used to avoid obstruction of the contralateral ducts which is insertion of a 7 French plastic stent alongside the metallic stent.

Interventions

All procedures will be performed under propofol sedation. Strictures will be identified by cholangiography and then dilated by a dilating balloon (diameter 6-10mm). A 4-6cm fully covered expandable metallic stent (Kaffes stent, Taewoong medical, Seoul, Korea) will then be deployed at the level of the stricture. In cases close to the hepatic hilum where the deployment of the stent is expected to reach one duct and possibly block another duct, a 7 Fr stent will be inserted prior to deployment of the metallic stent in the contralateral duct.. \- Stent will be extracted endoscopically after 6 months.

Strictures will be identified by cholangiography and then dilated by a dilating balloon (diameter 6-10mm). A 10 French plastic stent will be inserted bypassing the level of the stricture. Stent replacement and the addition of further stents will be planned after 3 months from the initial procedure and every 3 months until stricture resolution occurs with a maximum of four procedures. Balloon dilatation with a 6-10 mm balloon will be used in each session before stent insertion.

Sponsors

Theodor Bilharz Research Institute
CollaboratorOTHER
National Hepatology & Tropical Medicine Research Institute
CollaboratorOTHER_GOV
Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Confirmed benign postsurgical biliary stricture by presence of all 3 of the following: Ultrasound imaging or Magnetic resonance cholangiopancreatography (MRCP) showing biliary dilatation, Raised bilirubin and or alkaline phosphatase, History of biliary tree surgery within the previous year * Naïve to endoscopic therapy * Age \> 18 years

Exclusion criteria

* Coagulopathy * Inability of patient to adhere to regular follow-up * Living-donor liver transplant patients

Design outcomes

Primary

MeasureTime frameDescription
Clinical success6 months after removal of stentsProportion of patients with Absence of clinical or laboratory evidence of recurrence of biliary obstruction

Secondary

MeasureTime frameDescription
Technical successAt time of procedureProportion of patients with Successful deployment of stents
Stricture resolution at end of treatmentAfter 6 months in the metallic stent group and after 12 or 15 months in the multiple plastic stents groupRadiological resolution of the stricture at the time of removal of the stents (after insertion of 3 or 4 stents) and after removal of the metallic stent.
Occurrence of complicationsup to 6 months after the last procedureoccurence of any procedure-related complication

Countries

Egypt

Contacts

Primary Contacthany shehab, FRCP
h.shehab@kasralainy.edu.eg+201111111071
Backup ContactYasser eltabbakh, MD
yass.tabakh@gmail.com+201001860999

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026