Cardiovascular Diseases Clinical Trial
Official title:
Favourable and Unfavourable Health Effects of Risk-Reducing Salpingo-Oophorectomy in Women With a High Genetic Risk of Ovarian Cancer
Risk-Reducing Salpingo-Oophorectomy (RRSO) at the age of 35 to 45 years is recommended for
women with a high genetic risk for ovarian cancer. While this procedure decreases the risk of
ovarian cancer by 80-96%, it also results in an immediate menopause. Current research on
potential adverse effects of premenopausal risk-reducing salpingo-oophorectomy, such as
increased risk of cardiovascular disease, compromised bone health, cognitive dysfunction and
reduced quality of life, is limited, mostly due to short follow up.
The investigators will conduct a multicenter cross-sectional study nested in a cohort of BRCA
mutation carriers from 8 Dutch centers for hereditary cancer. Eligible participants are women
who underwent RRSO before the age of 45. The participants will be frequency-matched on
current age with women above the age of 55 without RRSO or with RRSO after the age of 55.
Participants will complete an online questionnaire containing various questions about
lifestyle, medical history, risk factors for cardiovascular disease, bone health, cognition
and quality of life. Participants will be asked to visit one of the participating hospitals
for a blood test, a cardiovascular assessment and a DEXA scan for determining bone mineral
density. Afterwards participants will be requested to perform the online Amsterdam Cognition
Scale.
Rationale: Women at high genetic risk of ovarian cancer are advised to undergo risk-reducing
salpingo-oophorectomy (RRSO) at ages 35-45 years. Currently, in the Netherlands ~500 women/
year opt for RRSO, which minimizes ovarian cancer risk and may decrease breast cancer (BC)
risk as well, due to reduced gonadal hormone levels. Besides favorable effects of RRSO on
ovarian cancer and, potentially, BC risk, RRSO induces immediate menopause, which may have
unfavorable long-term health consequences. Early menopause has been associated with increased
risks of cardiovascular disease (CVD), lower bone mineral density (BMD), cognitive
impairment, and decreased quality of life. Current evidence regarding these health effects is
mainly based on women with a natural early menopause, and it is unknown whether these results
hold for women undergoing RRSO at early premenopausal ages.
Objective: The investigators will investigate long-term health effects of premenopausal RRSO
on (subclinical) cardiovascular status, BMD, cognition and quality of life.
Study design: the investigators will assess long-term health effects of RRSO in a
cross-sectional study, among 500 women who underwent premenopausal RRSO compared to 250 women
of the same age without RRSO (or with RRSO after age 55). Eligible women will be invited to
participate in a screening program assessing cardiovascular status, bone mineral density,
cognitive functioning and quality of life.
Study population: Women are eligible for the premenopausal RRSO group if:
- RRSO before the age of 45 years;
- RRSO was done 10 or more years ago; Women are eligible for the comparison group without
premenopausal RRSO if the participant did not undergo RRSO before the age of 55 years,
and did not have a natural or therapy induced menopause before age 50.
Primary study outcome: To study long-term effects of premenopausal RRSO on:
- (subclinical) CVD
- BMD
- Cognition
Secondary study outcome: To study long-term effects of premenopausal RRSO on:
- Quality of life
- Urogenital problems
- Cardiovascular risk factors
Furthermore, the investigators will examine the influence of age at RRSO, time since RRSO,
hormone replacement therapy (HRT), carrier ship of a BRCA1 or BRCA2 mutation and BC history
on the outcome.
The obtained knowledge will assist physicians in counselling women with high ovarian cancer
risk and help them to make well-informed decisions.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05654272 -
Development of CIRC Technologies
|
||
| Recruiting |
NCT05650307 -
CV Imaging of Metabolic Interventions
|
||
| Recruiting |
NCT04515303 -
Digital Intervention Participation in DASH
|
||
| Completed |
NCT04056208 -
Pistachios Blood Sugar Control, Heart and Gut Health
|
Phase 2 | |
| Recruiting |
NCT04417387 -
The Genetics and Vascular Health Check Study (GENVASC) Aims to Help Determine Whether Gathering Genetic Information Can Improve the Prediction of Risk of Coronary Artery Disease (CAD)
|
||
| Not yet recruiting |
NCT06211361 -
Cardiac Rehabilitation Program in Patients With Cardiovascular Disease
|
N/A | |
| Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
| Recruiting |
NCT04514445 -
The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches.
|
||
| Enrolling by invitation |
NCT04253054 -
Chinese Multi-provincial Cohort Study-Beijing Project
|
||
| Completed |
NCT03273972 -
INvestigating the Lowest Threshold of Vascular bENefits From LDL Lowering With a PCSK9 InhibiTor in healthY Volunteers
|
N/A | |
| Completed |
NCT03680638 -
The Effect of Antioxidants on Skin Blood Flow During Local Heating
|
Phase 1 | |
| Recruiting |
NCT04843891 -
Evaluation of PET Probe [64]Cu-Macrin in Cardiovascular Disease, Cancer and Sarcoidosis.
|
Phase 1 | |
| Completed |
NCT04083846 -
Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of High-dose CKD-385 in Healthy Volunteers(Fed)
|
Phase 1 | |
| Completed |
NCT04083872 -
Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of Highdose CKD-385 in Healthy Volunteers(Fasting)
|
Phase 1 | |
| Completed |
NCT03693365 -
Fluid Responsiveness Tested by the Effective Pulmonary Blood Flow During a Positive End-expiratory Trial
|
||
| Completed |
NCT03619148 -
The Incidence of Respiratory Symptoms Associated With the Use of HFNO
|
N/A | |
| Completed |
NCT03466333 -
Postnatal Enalapril to Improve Cardiovascular fUnction Following Preterm Pre-eclampsia
|
Phase 2 | |
| Completed |
NCT04082585 -
Total Health Improvement Program Research Project
|
||
| Completed |
NCT05132998 -
Impact of a Comprehensive Cardiac Rehabilitation Program Framework Among High Cardiovascular Risk Cancer Survivors
|
N/A | |
| Completed |
NCT05067114 -
Solutions for Atrial Fibrillation Edvocacy (SAFE)
|