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

NCT ID: NCT00625248

Last Updated: 2013-06-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

12000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-02-29

Study Completion Date

2010-01-31

Brief Summary

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

Detailed Description

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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.

Conditions

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Bleeding

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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no anthithrombotic

procedures where there were no antithrombotics

Antithrombotics

Intervention Type DRUG

With or without or discontinuted use of Antithrombotics

Antithrombotic - continued

patients who are on antithrombotics

Antithrombotics

Intervention Type DRUG

With or without or discontinuted use of Antithrombotics

Discontinued Antithrombotic

Patients who were on antithrombotics but have been discontinued

Antithrombotics

Intervention Type DRUG

With or without or discontinuted use of Antithrombotics

Interventions

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Antithrombotics

With or without or discontinuted use of Antithrombotics

Intervention Type DRUG

Other Intervention Names

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anticoagulant or antiplatelet drugs

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pain Management Center of Paducah

OTHER

Sponsor Role lead

Responsible Party

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Laxmaiah Manchikanti, MD

Medical Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Laxmaiah Manchikanti, MD

Role: PRINCIPAL_INVESTIGATOR

Ambulatory Surgery Center, Paducah

Locations

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Pain Management Center of Paducah

Paducah, Kentucky, United States

Site Status

Countries

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United States

References

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Manchikanti L, Malla Y, Wargo BW, Cash KA, McManus CD, Damron KS, Jackson SD, Pampati V, Fellows B. A prospective evaluation of bleeding risk of interventional techniques in chronic pain. Pain Physician. 2011 Jul-Aug;14(4):317-29.

Reference Type RESULT
PMID: 21785475 (View on PubMed)

Manchikanti L, Malla Y, Wargo BW, Fellows B. Infection control practices (safe injection and medication vial utilization) for interventional techniques: are they based on relative risk management or evidence? Pain Physician. 2011 Sep-Oct;14(5):425-34.

Reference Type DERIVED
PMID: 21927046 (View on PubMed)

Other Identifiers

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protocol 18

Identifier Type: -

Identifier Source: org_study_id

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