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A randomized controlled trial for vaginal CO2 laser therapy for female sexual dysfunction in childbearing age women

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Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021657
Enrollment
Unknown
Registered
2019-03-03
Start date
2017-09-01
Completion date
Unknown
Last updated
2019-03-04

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

Conditions

Female sexual dysfunction

Interventions

Experimental group:CO2 laser therapy
control group:Kegel exercises

Sponsors

Dept of O/G, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing, China
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) with regular menstrual cycle; (2) be in good physical conditions; (3) having normal cognitive ability; (4) heterosexual; (5) married or having long-term partners; (6) defined as at high risk of sexual dysfunction by the Chinese version of the Women's Sexual Function Index (CVFSFI) if the total score=26.55.

Exclusion criteria

Exclusion criteria: (1) be widowed, divorced or separated; (2) having a history with genital tract malformation; (3) with incompletely urinary incontinent and/or symptomatic pelvic organ prolapse; (4) having a history with mesh implantation surgery in the pelvic floor; (5) having acute pelvic inflammatory disease; (6) with gynecological malignant tumors; (7) abnormal TCT screening results; (8) be in pregnancy or the puerperium.

Design outcomes

Primary

MeasureTime frame
CVFSFI scores;

Countries

China

Contacts

Public ContactZhu Lan

Dept of O/G, Peking Union Medical College Hospital, Chinese Academy of Medical Science

zhu_julie@vip.sina.com+86 10 65296784,(8610) 13911714696

Outcome results

None listed

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