Investigating the effect of hydroalcoholic extract of Stachys lvandulifolia on hot flashes in menopausal wome

Phase 3

Recruiting

Conditions: Hot flashes in menopausal women.
Menopausal and female climacteric states
N95.1

Registration Number: IRCT20240211060955N1

Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 86

Inclusion Criteria

Iranian and resident of Yasouj
Being literate in reading and writing
Willing to participate in research
Women aged 45-60
Duration of menopause at least 1 and at most 5 years
Absence of menopause at ages younger than 40 years old
Pap smear test is normal
Complaining of hot flashes
Not using tobacco and alcohol
Not suffering from physical diseases
Not suffering from mental diseases according to the statement of the research unit
Not suffering from infectious and febrile diseases
No unfortunate and stressful events in life in the past 6 months
No depression, stress or severe anxiety
No use of treatments such as hormone therapy, food supplements, medicinal plants containing phytoestrogens, etc. in the Previous 6 months for Relieving the side effects of menopause
Not taking drugs that affect vasomotor symptoms such as veraliprid, clonidine within 3 months before entering Research
No contraindications to hormone use
Body mass index less than 30

Exclusion Criteria

Reluctance to continue participating in the research.
Suffering from febrile diseases during the study
Simultaneous participation in another clinical trial
Hospitalization for any reason during the research period
Occurrence of any possible complications during the research period
Consumption of soy or its products during the study
Failure to take the drug for 4 consecutive doses or 6 alternating doses.
Occurrence of a severe stressful event during the study

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of hot flashes. Timepoint: One week before the start of the intervention and in the 2nd and 4th weeks after the intervention. Method of measurement: Daily hot flush registration form.;Intensity of hot flashes. Timepoint: One week before the start of the intervention and in the 2nd and 4th weeks after the intervention. Method of measurement: Daily hot flush registration form.;Number of hot flashes during the day. Timepoint: One week before the start of the intervention and in the 2nd and 4th weeks after the intervention. Method of measurement: Daily hot flush registration form.

Secondary Outcome Measures