Comparison of Sexual Function Before and After Using a Pessary in Women with Pelvic Floor Disorders

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20101222005448N4

Enrollment

Registered

2019-01-21

Start date

2018-09-06

Completion date

Unknown

Last updated

2019-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prolapse Of Pelvic Organs. Female genital prolapse

Interventions

Intervention group: Put a pessary into the vagina, Made in America, mylex brand, Approved by America FDA.

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Satisfaction to participate in the study The ability to have sex Married Age 18 and above Pelvic floor disorders that do not have surgical indication

Exclusion criteria

Exclusion criteria: Having a history of chronic diseases (diabetes - high blood pressure - heart disease) affecting sexual function (in each of the couples) Sexual problems in the spouse such as premature ejaculation and impotence Drinking alcohol (in each of the couples)

Design outcomes

Primary

Measure	Time frame
Sexual function. Timepoint: Before intervention; ?wo weeks after the intervention; three months afte rintervention. Method of measurement: International Prolaps-Urrinary Incontinenc Sexual Function(PISQ-12).	—

Secondary

Measure	Time frame
Quality of life. Timepoint: Before intervention; ?wo weeks after the intervention; three months afte rintervention. Method of measurement: International Prolapse-Urinary Incontinence Sexual Function(PISQ-12).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme Mallah

Tabriz University of Medical Sciences

lahroudin@gmail.com+98 41 3553 9161

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026