Health Assessment Study (0954-946)

NCT ID: NCT00541684

Last Updated: 2024-08-15

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

143 participants

Study Classification

INTERVENTIONAL

Study Start Date

2001-07-11

Study Completion Date

2003-01-23

Brief Summary

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The study will look at the effects of losartan or atenolol on frequency of sexual intercourse in subjects with newly diagnosed mild to moderate hypertension.

Detailed Description

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Conditions

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Hypertension

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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MK0954, /Duration of Treatment : 16 Weeks

Intervention Type DRUG

Comparator : atenolol /Duration of Treatment : 16 Weeks

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Newly diagnosed with mild to moderate hypertension\\
* Married male in stable heterosexual relationship
* No prior history of sexual dysfunction
* Satisfied with overall sex life
* Patient's spouse is in close proximity for the study
* Has had at least 2 but not more than 10 sexual intercourse events during the 2 week period prior to study start
* Patient able to visit doctor in the morning of each scheduled visit
* Able to complete the self administered health assessment questionnaire

Exclusion Criteria

* Hypertension due to cancer, history of heart or circulatory problems
* History of mental disorder that might impair sexual function
* History or presence of drug or alcohol abuse
* Prior surgery for erectile dysfunction or other urological procedure
* No penile implant or assist devices
* History of chronic liver disease, history of diabetes
* History of severe life-threatening diseases such as, cancer, AIDS or positive HIV test
* Subjects with only 1 kidney
* Mental handicap or legal incapacity
Minimum Eligible Age

40 Years

Maximum Eligible Age

49 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Organon and Co

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

Other Identifiers

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2007_624

Identifier Type: -

Identifier Source: secondary_id

0954-946

Identifier Type: -

Identifier Source: org_study_id

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