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Evaluation of the antioxidant effect of Rosmarinus officinalis in women

Evaluation of the antioxidant potential of Rosmarinus officinalis in women submitted to radiofrequency

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-86m4sns
Enrollment
Unknown
Registered
2022-02-17
Start date
2020-12-15
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

Anthropometry

Interventions

The 40 study participants will be divided into two groups: control and intervention. Both groups will receive the application of 12 aesthetic sessions with the Radio Frequency equipment, 3 times a wee
B01.650.940.800.575.912.250.583.520.757

Sponsors

Universidade Regional do Noroeste do Estado do Rio Grande do Sul
Lead Sponsor
Universidade Regional do Noroeste do Estado do Rio Grande do Sul
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Women from 18 to 50 years old; localized abdominal fat; do not present comorbidities: hypertension, diabetes and autoimmune diseases; have not performed non-invasive cosmetic procedures in the last 30 days; are not on a restrictive diet.

Exclusion criteria

Exclusion criteria: Incapable natural person; pregnant women; breastfeeding women; use of anti-inflammatory drugs; herbal medicines; slimming products; allergy or intolerance to Rosmarinus officinalis; radiofrequency sensitivity or allergies and contraindications; obese; who have performed invasive cosmetic procedures in the last 12 months; do not accept to participate in the research.

Design outcomes

Primary

MeasureTime frame
Rosmarinus officinalis antioxidant activity, evaluated through antioxidant enzymes, comparing control and intervention groups. To quantify the change in oxidative stress markers, laboratory techniques were used: Catalase, Superoxide Dismutase, Reactive Species to Thiobarbituric Acid and Non-Protein Thiols, through blood samples collected at the beginning and at the end of the study.

Secondary

MeasureTime frame
Secondary outcomes are not expected.

Countries

Brazil

Contacts

Public ContactUniversidade do Rio Grande do Sul

Universidade Regional do Noroeste do Estado do Rio Grande do Sul

unijui@unijui.edu.br+55(55)33320200

Outcome results

None listed

Source: REBEC (via WHO ICTRP)