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Combination of Laser Therapy and Phytotherapy for the Treatment of Menopausal Symptoms

The use of standardized extracts of Angelica keiskei and Panax ginseng as a strategy to potentiate the biological effects induced by red laser on postmenopausal symptoms

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
REBEC
Registry ID
RBR-10vj22fr
Enrollment
Unknown
Registered
2025-06-18
Start date
2024-05-05
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Menopause and female climacteric status

Interventions

This randomized, double-blind, comorbidity-stratified clinical trial will investigate the efficacy of red laser, the combination of Angelica keiskei and Panax ginseng (Angelica keiskei e Panax ginseng
E02.594.540

Sponsors

Centro de Ciências Biológicas e da Saúde da Universidade Federal de São Carlos
Lead Sponsor
Centro de Ciências Biológicas e da Saúde da Universidade Federal de São Carlos
Collaborator

Eligibility

Sex/Gender
Female
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: Women between 40 and 65 years of age; experiencing amenorrhea for at least 12 months due to natural causes or due to health treatment; characterizing the post-menopausal period

Exclusion criteria

Exclusion criteria: Participants who do not sign the informed consent form; women who have received hormone therapy in the last 6 months; with untreated hypothyroidism; any type of cancer; photosensitivity; cardiac arrhythmias; pacemaker wearers; presence of neurological; renal; hepatic diseases or infectious disease

Design outcomes

Primary

MeasureTime frame
Espera-se encontrar diminuição na pontuação na escala de avaliação da menopausa e dos biomarcadores inflamatórios

Secondary

MeasureTime frame
It has no secondary outcome.

Countries

Brazil

Contacts

Public ContactRita Alcântara

Universidade Federal de São Carlos- UFSCar

rita.cotta@estudante.ufscar.br+55(16)3351 - 8327.

Outcome results

None listed

Source: REBEC (via WHO ICTRP)