이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

조기 난소 기능 부전이있는 청소년의 호르몬 대체 요법

Background:

Premature ovarian insufficiency (POI) is a condition in which women under the age of 40 years have absent or irregular menstrual cycles. POI can cause infertility, signs of menopause, osteoporosis, and other symptoms. Hormone replacement therapy (HRT) is a treatment that gives women extra hormones, such as estrogen and progesterone. HRT works well in adult women. Researchers want to find the most effective doses and regimens for adolescents.

Objective:

To monitor the effects of HRT on adolescents with POI.

Eligibility:

Female adolescents aged 11 to 19 years diagnosed with POI. Healthy volunteers are also needed.

Design:

All participants will have clinic visits every 6 months for 2 years. Each visit may last 2 days. Each visit may include:

Blood and urine tests.

A test of their heart function.

A test to measure the stiffness of their blood vessels. Participants will lie flat with a blood pressure cuff on a leg and a meter on the neck while the cuff inflates.

A test of their grip strength. Participants will squeeze a handheld device as hard as they can.

Two scans to measure bone density. For one, participants will lie on a table while a scanner passes along their body. For the other, participants will sit in a chair and insert their forearm, then their lower leg, into a scanner.

A test to measure skin pigmentation. Participants' skin will be touched lightly with a device.

An optional visual exam of the vagina. Some vaginal fluid may also be collected with a cotton swab/cytobrush.

Participants with POI will receive HRT. They will be given estrogen patches and progesterone pills.

연구 개요

상세 설명

Study Description:

This is a study of adolescents with premature ovarian insufficiency (POI) and their response to hormone replacement therapy (HRT).

Objectives:

Primary:

To identify the phenotype and associated genotype of adolescents with POI at the time of diagnosis, including assessment of overall bone health of participants pre- and post-HRT treatment with respect to bone mineral density (BMD) and other skeletal endpoints.

Bone Health:

-Follow patients with POI for bone health assessments:

  • Measure BMD at different skeletal sites, including the central skeleton (lumbar spine, total body less head, and hip - femoral neck and total hip)
  • Perform vertebral fracture assessment (VFA)
  • Determine body composition of lean body and fat mass (total body) and correlate with BMD.
  • Assess skin pigmentation and muscle grip strength and correlate with BMD

Secondary:

Bone Health

-Follow patients with POI for bone health assessments:

  • Measure BMD at peripheral skeleton (radius and tibia)
  • Evaluate bone microarchitecture and strength of the radius and tibia.

Metabolic Phenotype:

  • Follow patients with POI for metabolic assessment:

    • Insulin resistance
    • Cardiovascular risk
    • Lipid profiles
    • Bone turnover

Muscle Phenotype:

-Follow patients with POI for muscle function assessment:

  • Determine hand grip muscle strength
  • Evaluate lean body mass (by DXA) to determine muscle mass

Cardiovascular Health

-Follow patients with POI for a cardiovascular evaluation:

  • Electrophysiologic parameters (from 12-lead EKG)
  • Arterial stiffness (by Pulse Wave Velocity, PWV)
  • Coagulation studies to determine the impact of HRT on clotting function

Genetic profiling:

-If obtained, assess the baseline genotype of patients with POI to correlate with BMD and other health outcomes

--If subjects are co-enrolled on NIAID protocol 17I0122, utilize that genetic sequencing data to associate with genotype and response of multiple health outcomes to HRT.

Quality of Life:

-Follow patients with POI for evaluation of an individual s perception of their life quality and health:

  • Evaluate the individual s perceived occupational performance in self-care, productivity, and leisure
  • Evaluate the individual s occupations or hobbies that align with their interests

Psychological health:

-Follow patients with POI for evaluation of an individual s mood and well-being:

  • Measure symptoms and severity of depression
  • Measure the state and trait components of anxiety

Menopause profile:

-Follow patients with POI for determining signs and symptoms of menopause:

  • Evaluate reproductive hormonal changes
  • Assess menopausal symptoms and their severity
  • Evaluate vaginal health

Hormone Replacement Therapy:

-Follow patients with POI longitudinally to determine the most effective HRT management:

  • Evaluate dosage, delivery, combination of HRT
  • Evaluate effects of HRT on bone, cardiovascular, metabolic, gynecologic, and psychological health

Endpoints:

Primary:

Longitudinal evaluation of BMD of the central skeleton (lumbar spine).

As secondary measures of bone health, dual-energy x-ray absorptiometry (DXA) measures of skeletal sites other than the spine (DXA - hip/total body) will be evaluated longitudinally in POI participants and their BMD compared to healthy control participants. Using DXA, vertebral fractures assessment (VFA) will be performed in POI participants and compared to healthy control participants. In addition, BMD will be evaluated with respect to skin pigmentation and muscle grip strength.

Secondary:

  • High-resolution peripheral quantitative computed tomography (HRpQCT) bone density and strength measures by HRpQCT of the peripheral skeleton (radius and tibia) will be evaluated longitudinally in participants with POI and their BMD compared to healthy control participants.
  • Compare metabolic and cardiovascular parameters in participants with POI to healthy controls.
  • Compare muscle phenotype in participants with POI to healthy controls by measuring muscle strength using hand grip dynamometry and measuring lean body mass (as measure of total body muscle mass) by DXA.
  • Compare repolarization changes (by 12-lead EKG), arterial stiffness (by PWV) and coagulation parameters in participants with POI to healthy controls.
  • Compare genetic background of participants with POI to healthy controls using whole genome sequencing.
  • Evaluate quality of life with Canadian Occupational Performance Measure (COPM) and Interest Checklist questionnaires.
  • Evaluate psychological health of participants with POI compared to healthy controls using the Beck Depression Inventory and Spielberger State/Trait Anxiety Inventory.
  • Evaluate menopausal profile in participants with POI compared to healthy controls by detecting changes in ovarian hormonal levels and correlating with responses on the Menopause Rating Scale, and vaginal cytology and degree of atrophy after HRT compared to baseline (and participants vs. controls).
  • Compare health effects from a typical clinical HRT regiment over the course of 2 years of administration.

연구 유형

중재적

등록 (추정된)

185

단계

  • 3단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Maryland
      • Bethesda, Maryland, 미국, 20892
        • 모병
        • National Institutes of Health Clinical Center
        • 연락하다:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • 전화번호: TTY dial 711 800-411-1222
          • 이메일: ccopr@nih.gov

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

11년 (어린이, 성인)

건강한 자원 봉사자를 받아들입니다

예

연구 대상 성별

여성

설명

  • INCLUSION CRITERIA:

Inclusion Criteria for POI Participants

To be eligible to participate in this study, an individual must meet all the following criteria:

  1. Individuals aged 11-19 years, inclusive, at the time of enrollment.
  2. Diagnosis of premature ovarian insufficiency.
  3. Documentation of one elevated serum FSH measurement greater than the testing laboratory's upper reference range (for age/Tanner stage).
  4. Identify as female (i.e., sex assigned at birth)
  5. Negative pregnancy test.

Inclusion Criteria for Healthy Volunteers:

  1. Individuals aged 11-19 years.
  2. Identify as female (i.e., sex assigned at birth)
  3. Negative pregnancy test.
  4. Absence of known chronic disease

EXCLUSION CRITERIA:

Male participants are excluded from both study groups (POI and Healthy Volunteers) as POI affects only the female reproductive system, while pregnant participants are not eligible to have DXA or HRpQCT imaging for safety reasons.

Exclusion Criteria for POI participants:

An individual who meets any of the following criteria will be excluded from participation in this study:

  1. POI in the setting of Turner syndrome.
  2. Patients who screened positive for celiac disease.
  3. Receipt of any medications including HRT determined by the investigator to affect bone metabolism 3 months prior to enrollment.
  4. Any medical condition determined by the investigator to affect bone health will be excluded.
  5. Presence of a medical, psychiatric, or social condition which, in the opinion of the investigator, would place undue burden on the subject, NIH resources, or increase risk of participation.
  6. Report of sexual activity but refusal to use a copper intrauterine device or double barrier forms of contraception during the study.

Exclusion Criteria for Healthy Volunteers:

For healthy volunteers, all exclusion criteria will apply as for POI participants except for number 1.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위화되지 않음
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
간섭 없음: Healthy Participants

Healthy Control Participants

실험적: POI Patients

POI patients will be receiving transdermal 17 beta-estradiol and oral micronized progesterone.

Oral micronized progesterone will be added (100 mg/day for 12 days/month) in the event of spontaneous vaginal bleeding and/or at 12 months over the 2-year protocol.

participants with POI (n=85) will receive transdermal 17 beta-estradiol (beginning at a dose of 25 microgram/patch applied weekly), with the dose increased at 3 months to 50 microgram, and thereafter every 6 months to 75 and 100 microgram/patch for pubertal induction or estrogen replacement (with 100 microgram/patch representing a full adolescent or young adult estradiol dose). The continued escalation of the estradiol dose and patch strength will be guided by the clinical presentation and physical examination (by the PI or designated AI).

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Longitudinal evaluation of BMD of the central skeleton (lumbar spine).
기간: 2 years

measures of bone health, dual-energy x-ray absorptiometry (DXA) measures of skeletal sites other than the spine (DXA - hip/total body) will be evaluated longitudinally in POI participants and their BMD compared to healthy control participants. Using DXA, vertebral fractures assessment (VFA) will be performed in POI participants and compared to healthy control participants. In addition, BMD will be evaluated with respect to skin pigmentation and muscle grip strength.

2 years

2차 결과 측정

결과 측정
측정값 설명
기간
Evaluate bone density and strength of the radius and tibia in participants with POI and compare with healthy controls.
기간: 2 years

Bone Health - Evaluate bone density and strength of the radius and tibia in participants with POI and compare with healthy controls.

2 years
Compare metabolic and cardiovascular parameters between participants with POI and healthy controls.
기간: 2 years

Metabolic Phenotype - Compare metabolic and cardiovascular parameters between participants with POI and healthy controls.

2 years
Assess muscle strength and lean body mass in participants with POI compared to healthy controls.
기간: 2 years

Muscle Phenotype - Assess muscle strength and lean body mass in participants with POI compared to healthy controls.

2 years
Analyze heart repolarization, arterial stiffness, and coagulation parameters in participants with POI versus healthy controls.
기간: 2 years

Cardiovascular Health - Analyze heart repolarization, arterial stiffness, and coagulation parameters in participants with POI versus healthy controls.

2 years
Compare the genetic background of participants with POI to healthy controls using whole genome sequencing.
기간: 2 years

Genetic profiling - Compare the genetic background of participants with POI to healthy controls using whole genome sequencing.

2 years
Assess quality of life using COPM and Interest Checklist questionnaires.
기간: 2 years

Quality of Life - Assess quality of life using COPM and Interest Checklist questionnaires.

2 years
Evaluate psychological health using the Beck Depression Inventory and Spielberger State/Trait Anxiety Inventory.
기간: 2 years

Psychological Health - Evaluate psychological health using the Beck Depression Inventory and Spielberger State/Trait Anxiety Inventory.

2 years
Compare menopausal profile, including ovarian hormone levels and responses to the Menopause Rating Scale, between participants with POI and healthy controls.
기간: 2 years

Menopausal profile - Compare menopausal profile, including ovarian hormone levels and responses to the Menopause Rating Scale, between participants with POI and healthy controls.

2 years
Assess health effects of a typical clinical HRT regimen over two years.
기간: 2 years

Hormone Replacement Therapy - Assess health effects of a typical clinical HRT regimen over two years.

2 years

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Catherine M Gordon, M.D., Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 7월 17일

기본 완료 (추정된)

2031년 12월 1일

연구 완료 (추정된)

2031년 12월 31일

연구 등록 날짜

최초 제출

2025년 2월 25일

QC 기준을 충족하는 최초 제출

2025년 2월 27일

처음 게시됨 (실제)

2025년 2월 28일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 10월 29일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 10월 28일

마지막으로 확인됨

2026년 10월 27일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 계획 설명

All IPD that underlie results in a publication will be deposited into a data repository in line with NIH regulations.

IPD 공유 기간

In line with publication of results.

IPD 공유 액세스 기준

De-identified datasets used to generate results presented in manuscripts will be deposited into a repository that can be publicly accessible in line with NIH regulations. In compliance with ethical standards and institutional policies, other access to individual participant data will be governed by a structured data-sharing framework to ensure participant privacy and confidentiality. Access to IPD will be granted under a Data Use Agreement that specifies permissible uses, prohibits re-identification or further data sharing, and requires secure storage and handling of data. Access will be restricted to de-identified or coded datasets, with direct identifiers removed.

IPD 공유 지원 정보 유형

  • 수액
  • ANALYTIC_CODE

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다