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Prospective Evaluation of Bleeding Risk of Anticoagulant and Anti-platelet Therapy

P

Pain Management Center of Paducah

Status

Completed

Conditions

Bleeding

Treatments

Drug: Antithrombotics

Study type

Observational

Funder types

Other

Identifiers

NCT00625248
protocol 18

Details and patient eligibility

About

This study will evaluate bleeding risk and differences in outcomes in patients receiving and not receiving anticoagulant or antiplatelet therapy

Full description

  1. To evaluate bleeding risk in interventional procedures in patients with or without antiplatelet and/or anticoagulant therapy.
  2. To evaluate differences in outcomes in patients not receiving any anticoagulant or antiplatelet therapy compared to patients receiving various types of drugs with anticoagulant or antiplatelet therapeutic effects.
  3. To evaluate and compare the adverse event profiling all patients.

Enrollment

12,000 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects undergoing interventional techniques. Subjects who were able to give voluntary, written informed consent.

Exclusion criteria

  • All those things, patients on heparin, dextran, and low molecular heparin

Trial design

12,000 participants in 3 patient groups

no anthithrombotic
Description:
procedures where there were no antithrombotics
Treatment:
Drug: Antithrombotics
Antithrombotic - continued
Description:
patients who are on antithrombotics
Treatment:
Drug: Antithrombotics
Discontinued Antithrombotic
Description:
Patients who were on antithrombotics but have been discontinued
Treatment:
Drug: Antithrombotics

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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