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Hot Flash as a Marker of Cardiovascular Risk in Recent Postmenopause: Effects of Non-hormonal Treatments

Primary Purpose

Postmenopausal Flushing, Cardiovascular Risk Factor, Endothelial Dysfunction

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Paroxetine
Placebo oral capsule
Sponsored by
Rio de Janeiro State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postmenopausal Flushing focused on measuring postmenopause, paroxetine, endothelial dysfunction, blood pressure, heart rate variability, sleep quality, perceived stress, sleepiness

Eligibility Criteria

45 Years - 65 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Postmenopause
  2. Present hot flushes (note ≥ 3 on a scale of 0 to 10)

Exclusion Criteria:

  1. > 10 years of hypoestrogenism
  2. Smoking
  3. Diabetes mellitus or altered fasting glycemia in use of oral hypoglycemic agents or insulin
  4. BMI ≥ 35 Kg / m2
  5. Uncontrolled hypertension - blood pressure (BP) ≥ 140/90 mmHg
  6. Users of glucocorticoids, phytoestrogens, β-blockers, selective serotonin reuptake inhibitors (SSRIs), selective noradrenaline reuptake inhibitors (SNRIs), clonidine, gabapentin, pregabalin, cinnarizine, alphamethyldopa or any drugs with effects on the central nervous system;
  7. Uncompensated hypo or hyperthyroidism;
  8. Previous cardiovascular event history.

Sites / Locations

  • Universidade do Estado do Rio de Janeiro

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Paroxetine

Placebo

Arm Description

Paroxetine 7,5 mg - 1 pill/day for 12 weeks

Placebo oral capsule (corn starch) - 1 pill/day for 12 weeks

Outcomes

Primary Outcome Measures

Endothelial function in non invasive venous occlusion plethysmography
Forearm blood flow (ml/min per 100 ml)

Secondary Outcome Measures

Full Information

First Posted
April 18, 2017
Last Updated
April 10, 2018
Sponsor
Rio de Janeiro State University
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1. Study Identification

Unique Protocol Identification Number
NCT03149419
Brief Title
Hot Flash as a Marker of Cardiovascular Risk in Recent Postmenopause: Effects of Non-hormonal Treatments
Official Title
Endothelial, Autonomic and Pressure Effects of Paroxetine in Recent Postmenopause Women With Hot Flashes: a Randomized Placebo Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
March 1, 2016 (Actual)
Primary Completion Date
September 30, 2017 (Actual)
Study Completion Date
March 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rio de Janeiro State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
Hot flashes, vasomotor symptoms that affect many postmenopausal women, are associated with cardiovascular disease and endothelial dysfunction. Estrogen therapy, associated or not with progestogens, is the standard treatment for vasomotor symptoms and improves the endothelial function of postmenopausal women with hot flushes, even those with cardiovascular risk factors, such as hypertension. It is not known whether hot flushes are a cause for the development of endothelial dysfunction or are markers of this dysfunction, evidenced by estrogen deficiency, thus representing primitive target organ (vessel) lesion. Paroxetine was approved by the FDA as a non hormonal treatment for menopausal hot flashes. In this double-blind randomized clinical trial, the vascular effects of paroxetine at a dose of 7.5 mg / day, compared to placebo, during 12 weeks are evaluated.
Detailed Description
Paroxetine and placebo effects at baseline and after 12 weeks in endothelial, autonomic and pressure components of vascular function are evaluated. Non invasive venous occlusion plethysmography is used to study endothelial function; ambulatory blood pressure monitoring is used to study blood pressure variations during daytime and nocturnal descent; autonomic function is studied following sympathetic and parasympathetic parameters through heart rate variability. The effects of paroxetine and placebo are also evaluated on: daytime sleepiness (through Epworth Sleepiness Scale ), sleep quality (through Pittsburgh Sleep Quality Index), perceived stress (through Perceived Scale Stress). Biochemical and hormonal profiles including complete lipid profile, fasting glucose, insulin, estradiol, follicle stimulating hormone (FSH), luteinizing hormone (LH); inflammatory and oxidative stress markers are also studied.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postmenopausal Flushing, Cardiovascular Risk Factor, Endothelial Dysfunction
Keywords
postmenopause, paroxetine, endothelial dysfunction, blood pressure, heart rate variability, sleep quality, perceived stress, sleepiness

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
140 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Paroxetine
Arm Type
Active Comparator
Arm Description
Paroxetine 7,5 mg - 1 pill/day for 12 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo oral capsule (corn starch) - 1 pill/day for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Paroxetine
Intervention Type
Drug
Intervention Name(s)
Placebo oral capsule
Primary Outcome Measure Information:
Title
Endothelial function in non invasive venous occlusion plethysmography
Description
Forearm blood flow (ml/min per 100 ml)
Time Frame
12 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Postmenopause Present hot flushes (note ≥ 3 on a scale of 0 to 10) Exclusion Criteria: > 10 years of hypoestrogenism Smoking Diabetes mellitus or altered fasting glycemia in use of oral hypoglycemic agents or insulin BMI ≥ 35 Kg / m2 Uncontrolled hypertension - blood pressure (BP) ≥ 140/90 mmHg Users of glucocorticoids, phytoestrogens, β-blockers, selective serotonin reuptake inhibitors (SSRIs), selective noradrenaline reuptake inhibitors (SNRIs), clonidine, gabapentin, pregabalin, cinnarizine, alphamethyldopa or any drugs with effects on the central nervous system; Uncompensated hypo or hyperthyroidism; Previous cardiovascular event history.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ciciliana MZ Rech
Organizational Affiliation
Universidade do Estado do Rio de Janeiro- BioVasc laboratory
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ruth Clapauch, PhD
Organizational Affiliation
Rio de Janeiro State University
Official's Role
Study Chair
Facility Information:
Facility Name
Universidade do Estado do Rio de Janeiro
City
Rio de Janeiro
ZIP/Postal Code
20550-900
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
8843881
Citation
Taddei S, Virdis A, Ghiadoni L, Mattei P, Sudano I, Bernini G, Pinto S, Salvetti A. Menopause is associated with endothelial dysfunction in women. Hypertension. 1996 Oct;28(4):576-82. doi: 10.1161/01.hyp.28.4.576.
Results Reference
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PubMed Identifier
20080857
Citation
Bechlioulis A, Kalantaridou SN, Naka KK, Chatzikyriakidou A, Calis KA, Makrigiannakis A, Papanikolaou O, Kaponis A, Katsouras C, Georgiou I, Chrousos GP, Michalis LK. Endothelial function, but not carotid intima-media thickness, is affected early in menopause and is associated with severity of hot flushes. J Clin Endocrinol Metab. 2010 Mar;95(3):1199-206. doi: 10.1210/jc.2009-2262. Epub 2010 Jan 15.
Results Reference
background
PubMed Identifier
22132748
Citation
Lambrinoudaki I, Augoulea A, Armeni E, Rizos D, Alexandrou A, Creatsa M, Kazani M, Georgiopoulos G, Livada A, Exarchakou A, Stamatelopoulos K. Menopausal symptoms are associated with subclinical atherosclerosis in healthy recently postmenopausal women. Climacteric. 2012 Aug;15(4):350-7. doi: 10.3109/13697137.2011.618564. Epub 2011 Dec 1.
Results Reference
background
PubMed Identifier
27219834
Citation
Silveira JS, Clapauch R, Souza Md, Bouskela E. Hot flashes: emerging cardiovascular risk factors in recent and late postmenopause and their association with higher blood pressure. Menopause. 2016 Aug;23(8):846-55. doi: 10.1097/GME.0000000000000641.
Results Reference
background
PubMed Identifier
24806158
Citation
Orleans RJ, Li L, Kim MJ, Guo J, Sobhan M, Soule L, Joffe HV. FDA approval of paroxetine for menopausal hot flushes. N Engl J Med. 2014 May 8;370(19):1777-9. doi: 10.1056/NEJMp1402080. No abstract available.
Results Reference
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Hot Flash as a Marker of Cardiovascular Risk in Recent Postmenopause: Effects of Non-hormonal Treatments

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