Efficacy and Safety of Sage Tablets Compared to Placebo in Menopausal Patients With Hot Flushes and Sweating
Primary Purpose
Menopausal Hot Flushes
Status
Terminated
Phase
Phase 4
Locations
Switzerland
Study Type
Interventional
Intervention
Sage extract, 3400 mg , DER 1:17
Sponsored by
About this trial
This is an interventional treatment trial for Menopausal Hot Flushes focused on measuring menopause, hot flushes, hot flashes, salvia, sage, sweating
Eligibility Criteria
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
Sites / Locations
- Dr. M. Morger
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Sage tablets
Placebo
Arm Description
Sage extract, 3400 mg , DER 1:17, in once daily application over 12 weeks treatment phase
Placebo, matching the verum in size and appearance, in once daily application over 12 weeks treatment phase
Outcomes
Primary Outcome Measures
Change from Baseline Hyperhidrosis Disease Severity Scale
Secondary Outcome Measures
Change from Baseline Menopause Rating Scale / MRS
Change from Baseline Modified Dem Tect
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02032862
Brief Title
Efficacy and Safety of Sage Tablets Compared to Placebo in Menopausal Patients With Hot Flushes and Sweating
Official Title
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
Study Type
Interventional
2. Study Status
Record Verification Date
July 2015
Overall Recruitment Status
Terminated
Why Stopped
Insufficient recruitment rate
Study Start Date
December 2013 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
A. Vogel AG
4. Oversight
Data Monitoring Committee
No
5. Study Description
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
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Menopausal Hot Flushes
Keywords
menopause, hot flushes, hot flashes, salvia, sage, sweating
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
107 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sage tablets
Arm Type
Experimental
Arm Description
Sage extract, 3400 mg , DER 1:17, in once daily application over 12 weeks treatment phase
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo, matching the verum in size and appearance, in once daily application over 12 weeks treatment phase
Intervention Type
Drug
Intervention Name(s)
Sage extract, 3400 mg , DER 1:17
Primary Outcome Measure Information:
Title
Change from Baseline Hyperhidrosis Disease Severity Scale
Time Frame
Week 12
Secondary Outcome Measure Information:
Title
Change from Baseline Menopause Rating Scale / MRS
Time Frame
Week 12
Title
Change from Baseline Modified Dem Tect
Time Frame
Week 12
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
Dr. M. Morger
City
Saint Gallen
State/Province
St. Gall
ZIP/Postal Code
9000
Country
Switzerland
12. IPD Sharing Statement
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Efficacy and Safety of Sage Tablets Compared to Placebo in Menopausal Patients With Hot Flushes and Sweating
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