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SuspendedNCT00569413Updated Jun 10, 2010

A Combined Psycho-pharmacological and Brain Imaging Study of Human Sexuality

An observational study in Hypoactive Sexual Desire Disorder and Erectile Dysfunction, sponsored by Hadassah Medical Organization. Suspended. Open to participants aged 21 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2010-06-10.

Sponsored by Hadassah Medical Organization · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
40
Ages
21 Years to 65 Years
Sex
All
01

Study summary

The current study combines a molecular genetic perspective, self report and brain imaging to the study of human sexuality in control subjects and individuals from a sexual disorder clinic. The investigators hypothesize that the variability in components of the brain dopaminergic system expressed in the mesolimbic reward system can explain variability in human sexuality, especially in desire and pleasure associated with sex.

Read the detailed description

We intend to combine molecular genetics of the dopamine receptors (D2, D3 D4 and D5) and brain imaging using 11 C Raclopride in Positron Emission Tomography (PET). 11 C Raclopride is a ligand which binds to the dopamine receptor D2 and can measure dopamine release during pleasure or anticipatory reward associated with sex. The current proposal will measure changes in DRD2 receptor occupancy using 11 C Raclopride following explicit visual sexual desire cues in healthy control subjects and individuals who suffer from sexual dysfunction. This is in order to determine how individual genotypes modulate dopamine release in vivo in the human brain.

02

Conditions studied

  • Hypoactive Sexual Desire Disorder
  • Erectile Dysfunction

Keywords

  • Sex
  • brain imaging
  • dopamine
  • sexual disorder
03

In context

Erectile Dysfunction

682 studies on the registry are indexed under Erectile Dysfunction; 116 are open to participants now.

This study's planned enrollment of 40 is below the median of 130 across 115 observational studies indexed under Erectile Dysfunction.

Browse Erectile Dysfunction studies →

Lead sponsor

Hadassah Medical Organization is the lead sponsor of 659 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

A group of healthy volunteers from the general public. A group of patients who suffer from sexual disorder from a primary care clinic.

Inclusion criteria

  • Healthy volunteers and patients
  • Age 21-65
  • Male or female

Exclusion criteria

Exclusion Criteria:

  • Psychiatric diagnosis/psychosis
  • Neurological damage associated with loss of consciousness
  • Infectious disease HIV
  • Herpes
  • Syphilis
  • Hyperactivity treated with ritalin
  • Pregnant women
  • Under age
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
40 participants (estimated)

Groups and cohorts

  • 1

    Healthy control subjects (n=20) age 21-65 who do not suffer from a psychiatric diagnosis or neurological damage, are under age, or are pregnant women

  • 2

    20 patients who suffer from sexual disorder (reduced sexual desire or sexual function) from a sexual disorder clinic, age 21-65, without any other psychiatric disorder, neurological damage, are not under age or pregnant women.

06

What researchers measure

Primary outcomes

  1. Brain Imaging data of DRD2 receptor occupancy during watching a sex videotape and neutral videotape

    Time frame: 2 Brain imaging sessions a week apart

Secondary outcomes

  1. Questionnaire ratings of human sexuality, pleasure, and anticipatory reward

    Time frame: Taken during brain scans

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 10, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00569413
Lead sponsor
Hadassah Medical Organization
Collaborators
Ben-Gurion University of the Negev
First posted
Dec 7, 2007
Start date
Apr 2011
Primary completion
Oct 2011 (estimated)
Completion
Oct 2011 (estimated)
Last update
Jun 10, 2010

Study contacts

Aviv M Weinstein, Ph.D
principal investigator · Hadasah Medical Organization, Jerusalem Israel

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is suspended, as verified in Jun 2010. You cannot join it, but the record below documents what was studied.

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