Skip to content

Comparative Study of the effect of CO2 Fractional Laser and Vaginal Cream Premarine on improving sexual function in Postmenopausal women

Comparative Study of the effect of CO2 Fractional Laser and Vaginal Cream Premarine on improving sexual function in postmenopausal women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160916029835N3
Enrollment
50
Registered
2018-10-06
Start date
2017-08-07
Completion date
Unknown
Last updated
2018-11-05

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

Conditions

Sexual dysfunction in postmenopausal women. Postmenopausal atrophic vaginitis

Interventions

Intervention 1: Vaginal cream premarine one-third of the oplicator three nights a week for twelve weeks. Intervention 2: Vaginal laser co2 monthly for three months.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Having sexual activity Having single sex and monogamy The age range of 65-45 years Having Disparony and Sexual Complications associated with Vaginal Atrophy Women who have passed at least one year of their last menstrual period or women with high FSH 40 The presence of symptoms of vaginal atrophy There is a sexual problem during intercourse Consent to participate in the study

Exclusion criteria

Exclusion criteria: Use of any type of topical or systemic hormonal alternative therapist for 6 months before entering the study Use of vaginal lubrication within 30 days before entering the study Acute or chronic urinary tract infection Acute Genital Infections (Herpes Candida) Psychiatric disorders interact with the completion of the informed consent form Smoking

Design outcomes

Primary

MeasureTime frame
Sexual Function. Timepoint: At the beginning of the study and 3 months after the intervention. Method of measurement: Sexual function Questionnaire.

Secondary

MeasureTime frame
Improve disparony. Timepoint: At the beginning of the study and 3 months after treatment. Method of measurement: Questionnaire.;Improve orgasms. Timepoint: At the beginning of the study and 3 months after treatment. Method of measurement: Questionnaire.;Improve desire. Timepoint: At the beginning of the study and 3 months after treatment. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahereh Khalili Borujeni

Tehran University of Medical Sciences

khalilitahereh@ymail.com+98 21 61190

Outcome results

None listed

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