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Long Term Treatment of Patients With Major Depressive Disorder With MK0869 (0869-065)(COMPLETED)

NCT ID: NCT00048594

Last Updated: 2017-05-05

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

PHASE3

Total Enrollment

800 participants

Study Classification

INTERVENTIONAL

Study Start Date

2002-01-03

Study Completion Date

2003-12-22

Brief Summary

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A clinical study to determine the efficacy and safety of an investigational medication (MK0869) in the treatment of depression.

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Detailed Description

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The duration of treatment is 20 months.

Conditions

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Major Depressive Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Interventions

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aprepitant

Intervention Type DRUG

Comparator: placebo (unspecified)

Intervention Type DRUG

Other Intervention Names

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MK0869

Eligibility Criteria

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Inclusion Criteria

Patients with Major Depressive Disorder
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Medical Monitor

Role: STUDY_DIRECTOR

Merck Sharp & Dohme LLC

Study Documents

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Document Type: CSR Synopsis Link

View Document

Other Identifiers

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Formally-35MRB2

Identifier Type: -

Identifier Source: secondary_id

MK0869-065

Identifier Type: -

Identifier Source: secondary_id

2006_405

Identifier Type: -

Identifier Source: secondary_id

0869-065

Identifier Type: -

Identifier Source: org_study_id

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