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临床试验/NCT05678192
NCT05678192已完成1 期

Optimization of Management Tactics for Postmenopausal Patients in Need of Menopausal Hormone Therapy, Taking Into Account the Effect on the Parameters of the Immune System

Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年12月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Changing the assessment of quality of life using the WHO Brief Questionnaire for Quality of Life (WHOQOL-BREF)

研究概览

简要总结

The objective of the study is to evaluate the effect of menopausal hormone therapy on the parameters of the immune system. To do this, patients took blood to assess the immune status before the start of therapy and after 3 months.

An additional task is to assess the content of blood sex hormones before the start of therapy and after 3 months.

详细描述

A study of 60 perimenopausal and postmenopausal patients was included. The cohort was divided into groups depending on the treatment regimen.

Group 1 (n=20) received transdermal menopausal hormone therapy (MHT). Group 2 (n=20) received oral MHT.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
45 Years 至 59 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • age from 45 to 59;
  • phase of reproductive aging - perimenopause, postmenopause or surgical menopause (ovariectomy);
  • indications for prescribing MHT

排除标准

  • Absolute contraindications to MHT:
  • Bleeding from the genital tract of unknown origin
  • Breast and endometrial cancer
  • Acute hepatitis
  • Acute deep vein thrombosis
  • Acute thromboembolism
  • Cutaneous porphyria
  • HIV infection and other congenital and acquired immunodeficiencies;
  • Systemic connective tissue diseases;
  • Oncological diseases in history;
  • History of chemotherapy and/or radiation therapy;
  • Autoimmune diseases;
  • Acute diseases and exacerbation of chronic diseases during the last 3 months;
  • Reception of immunomodulatory drugs during the last 3 months.

研究组 & 干预措施

Transdermal MHT

Other

The group includes women 45-59 years old, with menopausal symptoms. The choice of transdermal MHT was based on personal history (chronic diseases of the gastrointestinal tract, high blood pressure, etc.), family history (stroke, thromboembolism in relatives, etc.), and patient preferences. Used estradiol hemihydrate 0.6 mg 2 protective pumps. The progesterone component of MHT includes micronized progesterone 100 mg or 200 mg, depending on the MHT regimen (continuous or cyclic). Blood sampling to determine the immune status is carried out before the start of therapy after 3 months.

干预措施: oral menopausal hormone therapy (Drug)

Transdermal MHT

Other

The group includes women 45-59 years old, with menopausal symptoms. The choice of transdermal MHT was based on personal history (chronic diseases of the gastrointestinal tract, high blood pressure, etc.), family history (stroke, thromboembolism in relatives, etc.), and patient preferences. Used estradiol hemihydrate 0.6 mg 2 protective pumps. The progesterone component of MHT includes micronized progesterone 100 mg or 200 mg, depending on the MHT regimen (continuous or cyclic). Blood sampling to determine the immune status is carried out before the start of therapy after 3 months.

干预措施: transdermal menopausal hormone therapy (Drug)

Oral MHT

Other

The group includes women 45-59 years old, with menopausal symptoms. Examination before the appointment of MHT can be carried out according to clinical recommendations. The choice of transdermal MHT was based on the history (chronic diseases of the gastrointestinal tract, high blood pressure, etc.), family history (stroke, thromboembolism in relatives, etc.), the patient's preferences.Drugs used in this group include:

Dydrogesterone 5 mg + Estradiol 1 mg or Dydrogesterone 10 mg + Estradiol 1 mg, depending on the MHT regimen. Blood sampling to determine the immune status is performed before the start of therapy and after 3 months

干预措施: oral menopausal hormone therapy (Drug)

Oral MHT

Other

The group includes women 45-59 years old, with menopausal symptoms. Examination before the appointment of MHT can be carried out according to clinical recommendations. The choice of transdermal MHT was based on the history (chronic diseases of the gastrointestinal tract, high blood pressure, etc.), family history (stroke, thromboembolism in relatives, etc.), the patient's preferences.Drugs used in this group include:

Dydrogesterone 5 mg + Estradiol 1 mg or Dydrogesterone 10 mg + Estradiol 1 mg, depending on the MHT regimen. Blood sampling to determine the immune status is performed before the start of therapy and after 3 months

干预措施: transdermal menopausal hormone therapy (Drug)

结局指标

主要结局

Changing the assessment of quality of life using the WHO Brief Questionnaire for Quality of Life (WHOQOL-BREF)

时间窗: 3 months

The WHO Brief Questionnaire for Quality of Life (WHOQOL-BREF) was used at baseline and 3 months later. The questionnaire includes 26 questions, from 1 to 5 points, where a higher score means a better result.

Evaluation of the severity of menopausal syndrome

时间窗: 3 months

The Green scale questionnaire was used initially and after 3 months against the background of menopausal hormone therapy. The questionnaire includes 21 questions from 0 to 3 points, where a lower score means a better result.

次要结局

  • Evaluation of the effect of therapy on the parameters of the immune status(3 months)

研究者

发起方
Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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