Clitoris Potential Analgesic Function Research by Pregnant Women : Feasibility Study

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

Completed

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Key information

Conditions

Pregnancy Related

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Rouen University Hospital

Rouen, France

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Vibrating Relaxation Tool

Other

Use of a Vibrating Relaxation Tool in case of pain during pregnancy

Primary outcomes

Acceptability

Time frame: through study completion, an average of 15 months

Among patients who had the information visit, proportion of those who were included and applied the procedure at least twice

Sponsors and collaborators

Lead sponsor

University Hospital, Rouen

Other

Registry information

Acronym: FAC

Important dates

Study start: 2020
Primary completion: 2022
Study completion: 2022
First posted: Feb 6, 2020
Registry last updated: May 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed