Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science

Outcome Measure:

Change from baseline in dryness related symptoms of genital mucous membranes

Outcome Description:

Interview for symptom score at baseline and study visits and a daily symptom logbook during the intervention

Outcome Time Frame:

Interviews at baseline, at 2 months, at 3 moths (end of intervention), and daily during the study (symptom logbooks)

Safety Issue:

No

Principal Investigator

Risto Erkkola, Professor

Investigator Role:

Principal Investigator

Investigator Affiliation:

Turun Gynekologikeskus, Turku, Finland

Authority:

Finland: Ethics Committee of the Hospital District of Southwest Finland

Study ID:

SBMM

NCT ID:

NCT01697085

Start Date:

October 2012

Completion Date:

May 2013

Related Keywords:

• Mucous Membranes
• sea buckthorn
• mucous membrane
• dryness
• metabolic syndrome
• vaginal atrophy
• Adenocarcinoma
• Adenocarcinoma, Mucinous
• Mucositis