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NCT04257318 Clinical Trial

Clitoris Potential Analgesic Function Research by Pregnant Women : Feasibility Study

Pregnancy Related Clinical Trial

— FAC  

Official title:
Clitoris Potential Analgesic Function Research by Pregnant Women : Feasibility Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04257318
Other study ID # 2018/0415/HP
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 11, 2020
Est. completion date November 2, 2022

Study information
Verified date January 2024
Source University Hospital, Rouen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Assessment of the acceptability by pregnant women on the research of the potential analgesic function of the clitoris.

Recruitment information / eligibility
Status Completed
Enrollment 32
Est. completion date November 2, 2022
Est. primary completion date November 2, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Pregnant woman, whatever the term, primiparous or multiparous - Age = 18 years old - Patient having read and understood the information letter and signed the consent form - Patient affiliated to Social Security Exclusion Criteria: - Inability to understand French or information, - Person deprived of their liberty by an administrative or judicial decision - Person placed under the protection of justice - Person under guardianship or curatorship

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Vibrating Relaxation Tool
Use of a Vibrating Relaxation Tool in case of pain during pregnancy

Locations
Country Name City State
France Rouen University Hospital Rouen

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Rouen

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Acceptability Among patients who had the information visit, proportion of those who were included and applied the procedure at least twice through study completion, an average of 15 months
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