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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03002948
Other study ID # ECTO
Secondary ID
Status Enrolling by invitation
Phase N/A
First received March 24, 2016
Last updated December 21, 2016
Start date April 2016
Est. completion date December 2017

Study information

Verified date December 2016
Source Bezmialem Vakif University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Observational

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 42
Est. completion date December 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Sexually active women between 18 and 50 years old

- BMI below 40 kg/m2

Exclusion Criteria:

- 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.

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Other:
Orgasm
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

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Bezmialem Vakif University

Outcome

Type Measure Description Time frame Safety issue
Primary orgasm score 12 weeks No
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