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Efficacy and Safety of Sage Tablets Compared to Placebo in Menopausal Patients With Hot Flushes and Sweating

Multicentric, Randomized, Double Blind Study for Assessment of Efficacy and Tolerability of Sage Tablets Compared to Placebo in Menopausal Patients With Hot Flushes and Sweating

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02032862
Enrollment
107
Registered
2014-01-10
Start date
2013-12-31
Completion date
2015-07-31
Last updated
2015-07-21

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

Conditions

Menopausal Hot Flushes

Keywords

menopause, hot flushes, hot flashes, salvia, sage, sweating

Brief summary

Sage tablets ( 3400 mg extract from fresh sage leaves, DER 1:17) in a once daily application over 12 treatment weeks are compared against placebo in 200 menopausal patients with ≥ 5 hot flushes daily and a Hyperhidrosis Scale score ≥ 2

Interventions

DRUGSage extract, 3400 mg , DER 1:17

Sponsors

A. Vogel AG
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
50 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Menopausal since ≥ 1 year * ≥ 5 hot flushes /24 hours * Hyperhidrosis Scale score ≥ 2

Exclusion criteria

* Affections like asthma, COPD, depression, diabetes, epilepsy, hyper- and hypothyreosis, malign tumours

Design outcomes

Primary

MeasureTime frame
Change from Baseline Hyperhidrosis Disease Severity ScaleWeek 12

Secondary

MeasureTime frame
Change from Baseline Menopause Rating Scale / MRSWeek 12
Change from Baseline Modified Dem TectWeek 12

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026