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Combined Hormone Therapy, C-reactive Protein(CRP) Levels and Life Quality in Natural Menopause Women

K

Karadeniz Technical University

Status

Completed

Conditions

CRP
Menopause

Study type

Observational

Funder types

Other

Identifiers

NCT04424173
2007/25

Details and patient eligibility

About

This study aims to assess the effect of low dose combined estradiol and norethindrone acetate hormone therapy on serum CRP levels and life quality in natural menopause women. 45 natural menopause women who admitted to Karadeniz Technical University, Faculty of Medicine, Department of Obstetrics and Gynaecology for 1 year and diagnosed as menopause and planned to have hormone therapy for menopausal symptoms involved in this study. The serum CRP levels and vasomotor symptoms scores graded according to Blatt-Kupperman Index and life quality scores according to Menopause-Specific Quality of Life Questionnaire (MENQOL) in Turkish were recorded before and after (3 months later) low dose hormone treatment (1 mg Estradiol and 0.5 mg Norethindrone acetate).

Enrollment

45 patients

Sex

Female

Ages

45 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Accepting consent to participate in the research and signing the form;
  • Postmenopausal women 45-55 years old
  • not having had menstruation for the past 6 months;
  • Hormone results compatible with menopause (FSH> 20 milli-International unit(mIU) / mL, E2 <20 mIU / mL) and presence of vasomotor and/or menopausal symptoms (moderate to severe);
  • no systemic disease (Diabetes, hypertension, hyperlipidemia, ischemic heart disease), or no infectious disease in the past 2 weeks;
  • not taking any hormone therapy or medication for at least 2 months;
  • no contraindications for hormone therapy in routine menopause evaluation;
  • Willingness to take hormone therapy
  • No smoking.

Exclusion criteria

  • Any systemic disease (DM, HT, hyperlipidemia, ischemic heart disease) presence
  • Smoking
  • Contraindications for hormone therapy
  • Failure to follow-up
  • Inability to complete three months of hormone therapy
  • Stopping hormone therapy due to vaginal bleeding during hormone therapy

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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