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The clinical trial of efficacy analysis of the efficacy of matrix radiofrequency on female vaginal laxity

The clinical trial of efficacy analysis of the efficacy of matrix radiofrequency on female vaginal laxity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113461
Enrollment
Unknown
Registered
2025-11-28
Start date
2023-11-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Vaginal relaxation

Interventions

Treatment group:Matrix RF therapy

Sponsors

Zhujiang Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Women aged 22–65; 2. Volunteered to participate and signed informed consent; 3. Vaginal relaxation graded at stage 2 or above; 4. Pelvic floor muscle strength below the 26.5 score standard; 5. Have a history of sexual activity and are dissatisfied; 6. Able to communicate well with the researchers and comply with all trial requirements; 7. Normal blood pressure and heart rate; 8. No contraindications.

Exclusion criteria

Exclusion criteria: 1. Victims of sexual assault or domestic violence, or couples with marital discord; 2. Those with severe endocrine disorders, immune diseases, hematologic diseases, infectious diseases, kidney diseases, or other internal medical conditions, or those accompanied by infectious diseases; 3. Patients with a history of vaginitis, pelvic inflammatory disease, malformations, or tumors; 4. Patients with a history of pelvic organ surgery; 5. Those with acute local or systemic bacterial infections that cannot be effectively controlled; 6. Patients in shock or critically ill who cannot cooperate with procedures or evaluation of outcomes; 7. Patients with mental or neurological disorders who cannot cooperate with the doctor; 8. Other situations deemed unsuitable for participation in the study by the researcher (such as pregnancy, etc.).

Design outcomes

Primary

MeasureTime frame
Vaginal relaxation questionnaire;Pelvic floor muscle strength assessment;

Secondary

MeasureTime frame
Examination of the vaginal canal;Sexual satisfaction questionnaire;

Countries

China

Contacts

Public ContactXiangdong Qi

Zhujiang Hospital, Southern Medical University

751756123@qq.com+86 138 2841 8380

Outcome results

None listed

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