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
About this trial
This is an interventional basic science trial for Takotsubo Cardiomyopathy
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
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
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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