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Sympathetic and Vascular Function in Takotsubo Syndrome (SAFT)

Primary Purpose

Takotsubo Cardiomyopathy

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Metoprolol Injection
Saline
Sponsored by
Danderyd Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Takotsubo Cardiomyopathy

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: For patients: Diagnosis of Takotsubo cardiomyopathy For Controls: Matching age with Takotsubo patients Signed informed consent Exclusion Criteria: Coronary anathomy precluding intracoronary investigations Severe obstructive pulmonary disease Kidney failure with estimated glomerular filtration rate < 30 ml/min/m2 Active malignancy Pericarditis

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Placebo Comparator

    No Intervention

    Arm Label

    Takotsubo Control

    Takotsubo Intervention

    Control

    Arm Description

    Patients with Takotsubo receiving betablockade

    Patients with Takotsubo receiving placebo

    Control subjects

    Outcomes

    Primary Outcome Measures

    Resting MSNA
    Muscle sympathetic nerve activity during rest
    MSNA increase during CPT
    Muscle sympathetic nerve activity increase during cold pressor test

    Secondary Outcome Measures

    MSNA increase during CPT after intervention
    Muscle sympathetic nerve activity increase during cold pressor test after betablockade
    Hemodynamic changes during CPT
    Change in blood pressure

    Full Information

    First Posted
    January 26, 2023
    Last Updated
    March 3, 2023
    Sponsor
    Danderyd Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05768542
    Brief Title
    Sympathetic and Vascular Function in Takotsubo Syndrome
    Acronym
    SAFT
    Official Title
    Vacular Structure, Function and Sympathetic Activity in Takotsubo Syndrome
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2022
    Overall Recruitment Status
    Completed
    Study Start Date
    April 12, 2016 (Actual)
    Primary Completion Date
    March 23, 2022 (Actual)
    Study Completion Date
    January 23, 2023 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Danderyd Hospital

    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
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The primary objective of this prospective, observational study is to compare muscle sympathetic nerve activity at rest and during stress between female patients with Takotsubo syndrome and healthy, matched volunteers. Do Takotsubo patients have an increased sympathetic nerve activity compared to controls? Do Takotsubo patients have an exaggerated sympathetic nerve activity response to stress? Does the sympathetic nerve activity response to stress in Takotsubo change after receiving the beta blocking agent metoprolol? Participants will be examined with muscle sympathetic nerve activity recording in the peroneal nerve at rest and during cold pressor test. After intravenous injection with beta blocking agent (metoprolol) or placebo (saline) in a 1:1 randomized fashion, muscle sympathetic nerve recording at rest and during stress will be repeated.
    Detailed Description
    Female Takotsubo patients included in the SAFT (sympathetic and vascular function in Takotsubo syndrome) study will be invited to undergo microneurography recording of muscle sympathetic nerve activity (MSNA) at rest and during stress one week to two month after study inclusion. Responses to stress with and without the commonly used betablocking agent metoprolol will be compares. Microneurography will be performed in the morning after a light caffeine-free breakfast with the subject supine and awake. Any medication with a beta blocking agent will be discontinued 24 hours prior to examination. MSNA will be recorded by inserting a tungsten electrode into the sympathetic nerve fibres of the peroneal nerve, with simultaneous blood pressure and heart rate monitoring. MSNA recording will then continue during stress induced by placing one of the subjects hand in ice-cold water for 90 seconds (cold pressor test). After intravenous injection with beta blocking agent (metoprolol) or placebo (saline) in a 1:1 randomized fashion, MSNA recording at rest and during stress will be repeated. Age- and gender-matched healthy volunteers will be recruited as controls and examined similarly with microneurography at rest and during stress. MSNA recordings will be amplified, computerized and saved for further analyses. MSNA will be quantified as burst incidence (burst per 100 heartbeats), burst frequence (bursts per minute) and relative median burst amplitude (%). MSNA activity will be compared between Takotsubo patients and controls and before and after betablockade in Takotsubo patients.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Takotsubo Cardiomyopathy

    7. Study Design

    Primary Purpose
    Basic Science
    Study Phase
    Phase 1, Phase 2
    Interventional Study Model
    Parallel Assignment
    Model Description
    Control group for primary outcome
    Masking
    ParticipantOutcomes Assessor
    Masking Description
    Intervention single blinded to participant. Intervention blinded to person analyzing the MSNA.
    Allocation
    Randomized
    Enrollment
    31 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Takotsubo Control
    Arm Type
    Active Comparator
    Arm Description
    Patients with Takotsubo receiving betablockade
    Arm Title
    Takotsubo Intervention
    Arm Type
    Placebo Comparator
    Arm Description
    Patients with Takotsubo receiving placebo
    Arm Title
    Control
    Arm Type
    No Intervention
    Arm Description
    Control subjects
    Intervention Type
    Drug
    Intervention Name(s)
    Metoprolol Injection
    Intervention Description
    If heart rate below 60, give 5 mg IV. If heart rate above 60, give 5 mg IV and repeat until heart rate below 65 or 20 mg given in total or systolic blood pressure below 110 mmHg.
    Intervention Type
    Drug
    Intervention Name(s)
    Saline
    Intervention Description
    5 ml given IV
    Primary Outcome Measure Information:
    Title
    Resting MSNA
    Description
    Muscle sympathetic nerve activity during rest
    Time Frame
    During 5 minutes rest
    Title
    MSNA increase during CPT
    Description
    Muscle sympathetic nerve activity increase during cold pressor test
    Time Frame
    During the last 60 seconds of the CPT
    Secondary Outcome Measure Information:
    Title
    MSNA increase during CPT after intervention
    Description
    Muscle sympathetic nerve activity increase during cold pressor test after betablockade
    Time Frame
    During the last 60 seconds of the CPT
    Title
    Hemodynamic changes during CPT
    Description
    Change in blood pressure
    Time Frame
    During the last 60 seconds of the CPT

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: For patients: Diagnosis of Takotsubo cardiomyopathy For Controls: Matching age with Takotsubo patients Signed informed consent Exclusion Criteria: Coronary anathomy precluding intracoronary investigations Severe obstructive pulmonary disease Kidney failure with estimated glomerular filtration rate < 30 ml/min/m2 Active malignancy Pericarditis
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jonas 9, MD, PhD
    Organizational Affiliation
    Danderyd University Hospital and karolinska Institutet
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    Needs approval according to GDPR but PI positive to requests

    Learn more about this trial

    Sympathetic and Vascular Function in Takotsubo Syndrome

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