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Application of CO2 Fractional Laser to Improve the Symptoms of Vulvovaginal and Prolapse Atrophy in Postmenopausal Women Referring to Yas Hospital

Application of CO2 Fractional Laser to Improve the Symptoms of Vulvovaginal and Prolapse Atrophy in Postmenopausal Women Referring to Yas Hospital,97-98

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180409039247N2
Enrollment
100
Registered
2019-06-10
Start date
2018-05-22
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Vaginal dryness, irritation, pruritus, urinary symptoms and painful intercourse. THEY ARE SYMPTOMS

Interventions

Intervention group:The fractional microablative CO2 laser system (SmartXide 2 V 2 LR, Monalisa Touch, DEKA, Florence, Italy) was applied. Laser energy was transmitted through a vaginal probe, the frac

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: postmenopausal woman aged 45 to 65 years with symptoms of vaginal atrophy that lasts more than 24 months after menopause. Vaginal dryness, irritation, pruritus, urinary symptoms and painful intercourse

Exclusion criteria

Exclusion criteria: Hormone therapy (topical or systemic) in the last 12 months• Use of vaginal moisturizers and gels• Genitourinary infection (Vulvovaginitis)• Women who use psychotropic drugs• BMI higher than 35• Current cancer history• Abnormal Pap smear• Menopause induced by medication• History of steroid use• History of vaginal radiotherapy in the past

Design outcomes

Primary

MeasureTime frame
We expect the quality of life that measure with standard devices (The questionnaire of quality of life questionnaire (SF-12), the Incontinence Questionnaire-Short Form (ICIQ-SF), the Female Sex Function Index6- The Menopause-Specific Quality of Life) will change in our study. Timepoint: At the beginning of the study and 4 weeks after the last treatment. Method of measurement: standard questionnaire that are validated in Iran.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarjan Ghaemi

Tehran University of Medical Sciences

majan_ghaemi@yahoo.com+98 21 8885 3138

Outcome results

None listed

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