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The safety evaluation of endoscopic biopsy against patients receiving anticoagulatns and antiplatelet agents.

The safety evaluation of endoscopic biopsy against patients receiving anticoagulatns and antiplatelet agents. - The safety evaluation of endoscopic biopsy during antithrombotic therapy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003750
Enrollment
100
Registered
2010-06-16
Start date
2010-06-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Outpatients undergoing gastrointestinal endoscopy during antithrombotic therapy

Interventions

Endoscopic biopsy

Sponsors

Department of Endoscopy and Endoscopic Surgery, Graduate School of Medicine, The University of Tokyo.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (A)Medical need of gastrointestinal endoscopy. (B)Comorbidity requiring antithrombotic therapy. (C)Receiving anticoagulants and/or antiplatelet agents. (D)Informed consent. (E)Performance status(ECOG):0-2. (F)Scheduled blood test about two weeks after biopsy. (G)Outpatient.

Exclusion criteria

Exclusion criteria: (A)Strong possibility of lesions requiring more invasive procedures than biopsy. (B)During hospitalization. (C)Other severe comorbidities. (D)During anticancer chemotherapy. (E)Severe hematological, hepatological, or renal disorder accompanied with hemorrhagic tendency. (F)INR exceeding the upper limit shown in the guideline by Japanese circulation society.

Design outcomes

Primary

MeasureTime frame
Gastrointestinal bleeding during two weeks after biopsy.

Countries

Japan

Contacts

Public ContactSatoshi Ono

Graduate School of Medicine, The University of Tokyo. Department of Gastroenterology.

satoshi-tky@umin.ac.jp

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026