NCT03002948

Brief Summary

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
42

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Apr 2016

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 24, 2016

Completed
8 days until next milestone

Study Start

First participant enrolled

April 1, 2016

Completed
9 months until next milestone

First Posted

Study publicly available on registry

December 26, 2016

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2017

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2017

Completed
Last Updated

December 26, 2016

Status Verified

December 1, 2016

Enrollment Period

1 year

First QC Date

March 24, 2016

Last Update Submit

December 21, 2016

Conditions

Sexual Dysfunction

Outcome Measures

Primary Outcomes (1)

  • orgasm score

    12 weeks

Study Arms (1)

Low orgasm

Female Sexual Function Index orgasm score below 3.6

Other: Orgasm

Interventions

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

Low orgasm

Eligibility Criteria

Age18 Years - 50 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

sexually active women

You may qualify if:

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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Sexual Dysfunction, Physiological

Condition Hierarchy (Ancestors)

Genital DiseasesUrogenital Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD

Study Record Dates

First Submitted

March 24, 2016

First Posted

December 26, 2016

Study Start

April 1, 2016

Primary Completion

April 1, 2017

Study Completion

December 1, 2017

Last Updated

December 26, 2016

Record last verified: 2016-12

Data Sharing

IPD Sharing
Will not share