Skip to content

Treatment of Postsphincterotomy Bleeding With a Novel Self-assembling Peptide Hemostatic Gel.

Treatment of Immediate and Prevention of Delayed Bleeding After Endoscopic Retrograde Cholangiopancreatography Sphincterothomy or Precut With a Novel Self-assembling Peptide Hemostatic Gel. A Single Centre Prospective Observational Nonrandomized Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05886127
Acronym
ERCPURA
Enrollment
80
Registered
2023-06-02
Start date
2022-08-01
Completion date
2023-10-30
Last updated
2023-06-02

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

Conditions

Biliary Obstruction, Complication of Treatment

Keywords

ERCP, A novel haemostatic agent, Postsfincterothomy bleeding

Brief summary

The aim of this observational study is to evaluate safety and efficacy of a novel self-assembling peptide hemostatic gel in reduction of bleeding after endoscopic sphincterotomy during ERCP (endoscopic retrograde cholangiopancreatography )

Detailed description

ERCP with sfincterotomy or precut is connected with procedural or/and postprocedural bleeding. Estimated risk of bleeding is from 2% to 10%. Procedural bleeding is usually managed by diluted epinephrine injection, balloon tamponade, hemoclip or fully covered metalic self-expanding stent placement. There is no standard preventive treatment for patients with higher risk of delayed post-sphincterotomy bleeding. PuraStat®, 3D Matrix Europe SAS, Caluire-et-Cuire, France) is synthetic self-assembling peptide haemostatic gel indicated to stop bleeding from small blood vessel or oozing from capillaries. Purastat® is easily aplicated through a catheter during the ERCP procedure and it is not significantly prolonging the procedure. The transparent gel is not compromising the endoscopic view and enables to continue in procedure if necessary. All patients after ERCP sfincterotomy or precut will recieve Purastat® during the procedure Adverse events (bleeding, cholangoitis, pancreatitis) will be monitored during following 4 weeks (ambulatory after hospital discharge) This cohort will be compared to historical control, when Purastat® was not available tu use.

Interventions

DEVICEA novel hemostatic agent (Purastat®)

A novel hemostatic agent (Purasta®) will be applied on cutted ampulla of Vater

Sponsors

General University Hospital, Prague
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

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

Inclusion criteria

* . All patients indicated for ERCP with papilosphincterotomy or precut. * Participant is willing and able to give informed consent for participation in the study

Exclusion criteria

* Known allergy to a novel hemostatic agent * Gravidity * Inability to sign informed consent

Design outcomes

Primary

MeasureTime frame
Number of bleeding episodes after ERCP sfincterothomy or precutOne month

Secondary

MeasureTime frame
Number of nonbleeding complications after ERCP sfincterothomy or precutOne month

Countries

Czechia

Contacts

Primary ContactPetr Hrabak, MD
petr.hrabak@vfn.cz224962580

Outcome results

None listed

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