Effect of Desmopressin on Platelet Function in CKD Patients on Antiplatelet Drug

NCT ID: NCT01841515

Last Updated: 2013-05-13

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

Clinical Phase

PHASE1

Total Enrollment

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-08-31

Study Completion Date

2013-04-30

Brief Summary

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Prolonged Collagen/Epinephrine - closure time (CEPI-CT) indicates platelet dysfunction in CKD patients taking antiplatelet agent. The synthetic vasopressin derivative, Desmopressin (DDAVP) shortens the prolonged bleeding time and improves platelet dysfunction measured by in vitro closure time: CEPI-CT in uremic patients. Desmopressin also antagonizes the in vitro platelet dysfunction induced by GPIIb/IIIa inhibitors, clopidogrel and aspirin. The investigators designed a prospective study to evaluate the effect of desmopressin on platelet function, as measured by in vitro collagen/epinephrine - closure time, in uremic patients who were taking antiplatelet drugs.

Detailed Description

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Conditions

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Bleeding Tachycardia Dyspnea

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Desmopressin

Twenty five patients with chronic kidney disease and who were taking antiplatelet agents and needed an emergent catheter insertion for hemodialysis

Group Type EXPERIMENTAL

Desmopressin administration

Intervention Type DRUG

Interventions

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Desmopressin administration

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* adult uremic patients with one or more antiplatelet medication,
* prolonged collagen/epinephrine (CEPI) closure time,
* need for emergent hemodialysis and
* subsequent catheter insertion

Exclusion Criteria

* acute coronary syndrome,
* hemophilia, and nephrogenic diabetes insipidus,
* allergy against desmopressin
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Ulsan

OTHER

Sponsor Role lead

Responsible Party

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Soon Bae Kim, M.D., PhD.

Professor of Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Asan Medical Center

Seoul, Songpa-gu, South Korea

Site Status

Countries

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South Korea

Other Identifiers

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NCT00134031

Identifier Type: -

Identifier Source: org_study_id

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