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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00443027
Other study ID # A9001303
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date March 2007
Est. completion date October 2008

Study information

Verified date May 2019
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Pfizer developed Heat Wash-Out (HWO) system is a software controlled electromechanical system designed to measure vaginal wall blood flow. A small vaginal probe is attached to a control unit. Output data is collected on a PC. By measuring the clearance of heat from the heated probe, a direct measure of absolute blood flow can be obtained. The study will assess changes in vaginal blood flow across the menstrual cycle following visual sexual stimulation.


Description:

Medical Device Development


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date October 2008
Est. primary completion date October 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Pre-menopausal healthy women aged 18-45 with regular, natural menstrual cycles.

- Subjects must be void of Female Sexual Disorder.

Exclusion Criteria:

- Pregnant or lactating women

- Postmenopausal subjects

- Subjects with evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric or neurologic disease.

Study Design


Related Conditions & MeSH terms

  • Sexual Dysfunction, Physiological

Intervention

Device:
Vaginal Heat Wash-Out Device
No drug administered. Device tested three times with each subject.

Locations

Country Name City State
Australia Pfizer Investigational Site Dulwich South Australia
Australia Pfizer Investigational Site Nedlands Western Australia

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary To investigate differences in vaginal blood flow across the menstrual cycle following visual sexual stimulation. 28d
Primary To assess the safety and toleration of the heat washout device. 28d
Secondary To investigate changes in subjective acute sexual arousal following visual sexual stimulation across the menstrual cycle. 28d
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