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Sexual DysfunctionECTONCT03002948

Effect of Clitoris Location on Orgasm

An observational study of Sexual Dysfunction, run by Bezmialem Vakif University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Topography and location of clitoris and its parts may affect the orgasm Read more about this study

Who is it for?
Ages 18 to 50 years, women only
Conditions the study is for
Sexual Dysfunction
What is being tested?
Orgasm
How many people
42 participants
Where
No sites listed yet
Study dates
Apr 2016to Dec 2017
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 50 years
  • Women only
  • No healthy volunteers
  • Adult

Study population: sexually active women

Who may be able to join

  • Sexually active women between 18 and 50 years old
  • BMI below 40 kg/m2

Who cannot join

  • BMI over 40 mhg/m2,
  • Women younger than 18 years old
  • Virgins
  • No active sexual intercourse, women with
  • Handicapped to get lithotomy position
  • Active vulvar and vaginal infection
  • Psychiatric diseases
  • Drug usage that may cause sexual dysfunction, menopause.

About this study

Official title: Effect of Clitoris Topography on Orgasm

Topography and location of clitoris and its parts may affect the orgasm

Read the detailed description

Orgasm measurement via Orgasm domain of Female Sexual Function Index, clitoris volume, suprapubic angle, urethra-levator gap, suburethral triangle area measurement could made using 4 D transperineal ultrasonography. Clitoris fourchette distance, clitoris perineal body distance, clitoris urethra distance could made with special compasses.

Being tested
Orgasm
Medical subject headings
Sexual Dysfunction, Physiological

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • OrgasmOther

    clitoris volume, suprapubic angle, urethra-levator gap, suburethral triangle area measurement could made using 4 D transperineal ultrasonography. Clitoris fourchette distance, clitoris perineal body distance, clitoris urethra distance could made with special compasses.

    Female Sexual Function Index orgasm domain score

Study groups in NCT03002948
Study groupRoleWhat they receive
Low orgasmFemale Sexual Function Index orgasm score below 3.6
Receives: Other: Orgasm

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. orgasm score

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Dec 2016 (estimated)
  2. Study startApr 2016
  3. Primary completionApr 2017 (estimated)
  4. Study completionDec 2017 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
42 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03002948
Sponsor's protocol ID
ECTO
Acronym
ECTO
Status last verified
Dec 2016
First submitted
24 Mar 2016
Last updated
26 Dec 2016
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Sexual Dysfunction, run by Bezmialem Vakif University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 26 Dec 2016. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

orgasm score (time frame: 12 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Dec 2016.

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Effect of Clitoris Location on Orgasm (NCT03002948) | AzTrials