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In patients with PSC, endoscopic therapy of strictures aims to improve cholestasis by relieving the biliary obstruction via endoscopic biliary dilatation with consideration of plastic stents in strictures refractory to dilatation due to the risk of pancreatitis and cholangitis . Short term stents have been shown to have similar recurrence-free rates compared to dilatation in a randomised control trial; however, this was terminated after interim analysis due to higher rates of serious adverse events in the stent group. The long term benefits are unclear; however, it may lead to improved survival compared to predicted survival. In this group of patients with limited treatment options, biodegradable stents may provide an attractive additional treatment modality in the management of high grade strictures.
Research hypothesis
The use of biodegradable stents leads to remodelling of high grade strictures in patients with PSC with fewer interventions in comparison to balloon dilation alone with a comparable risk profile to current therapy.
Primary endpoint
Technical success and safety of biodegradable stent placement at ERC
Secondary endpoints
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Archimedes stent insertion | Experimental | Archimedes stent insertion at ERCP for patients with PSC and a HGS |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| archimedes stent | Device | archimedes stent for HGS |
|
| Measure | Description | Time Frame |
|---|---|---|
| Deployment of biodegradable stent placement across stricture at ERC in 20 patients | Deployment of stent across the stricture - yes or no | at time of primary ERC |
| Measure | Description | Time Frame |
|---|---|---|
| Cumulative recurrence -free rate of primary high grade strictures within 12 months. | has the stricture reoccured (yes or no) at 12 months post ERC and stent | through study completion up to 12 months |
| Change in symptoms as assessed by the Amsterdam cholestatic complaints score (ACCS) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| DEEPAK JOSHI, PhD | King's College Hospital NHS Trust | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| King's College Hospital, London | Recruiting | London | SE5 9RS | United Kingdom |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Apr 1, 2026 | May 9, 2026 | Prot_000.pdf |
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| ID | Term |
|---|---|
| D015209 | Cholangitis, Sclerosing |
| ID | Term |
|---|---|
| D002761 | Cholangitis |
| D001649 | Bile Duct Diseases |
| D001660 | Biliary Tract Diseases |
| D004066 | Digestive System Diseases |
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change in pruritus, fatigue, pain and fever |
| Post ERC to assessment at 2 weeks and 12 weeks, and at 12 months. |
| Clinical success is defined by improvement in liver function tests (LFT) by 20% at week 2 and week 12. | Change in liver blood tests: - ALP, AST, ALT, Bilirubin | At week 2 and 12 weeks post ERCP |
| Change in quality fo life as assessed by the Short form-36 (SF-36 | Change in QoL | after ERC and assesment at 2 weeks, 12 weeks and 12 months |
| Mortality over 12 months. | Death related to PSC | Within 12 months of primary ERCP |
| morbidity related to ERC | Complications including cholangitis and pancreatitis post ERC | within 12 months of ERC |
| stricture recurrence post ERC | Development of a stricture in the bile duct | 12 months post ERC |
| Development of ascites post erc | development of abdominal ascites post ERC | up to 12 months post ERC |
| Need for liver transplantation | patients who are assessed and then listed for liver transplant | up to 12 months following ERC |