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Heart Rate Variability and Hyperthyroidism: Evaluation of the Short-term Effects of Propanolol

Short Term Effects of Propanolol on Heart Rate Variability of Hyperthyroidism

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03393728
Enrollment
10
Registered
2018-01-08
Start date
2008-09-01
Completion date
2009-09-30
Last updated
2018-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperthyroidism

Keywords

hyperthyroidism, heart rate variability, propanolol, Africa

Brief summary

Objective: The aim of our study was to evaluate the short term effects of Propanolol on heart rate variability in patients with hyperthyroidism. Design: In ten patients newly diagnosed as having hyperthyroidism and naïve of all treatment specific for hyperthyroidism, we evaluated the short term effects of Propanolol on heart rate variability (HRV). Methods: We measured heart rate variability by power spectral analysis during 2 hours of rest and during Ewing's tests before and after the administration of Propanolol 40mg/12 hours orally for 72 hours.

Detailed description

Objective: The aim of our study was to evaluate the short term effects of Propanolol on heart rate variability in patients with hyperthyroidism. Design: In ten patients newly diagnosed as having hyperthyroidism and naïve of all treatment specific for hyperthyroidism, we evaluated the short term effects of Propanolol on heart rate variability (HRV). Methods: We measured heart rate variability by power spectral analysis during 2 hours of rest and during Ewing's tests before and after the administration of Propanolol 40mg/12 hours orally for 72 hours. Other outcomes included mean heart rate, mean R-R interval during 2-hour rest. The study questions the systematic adjunction of Propanolol early in the treatment of hyperthyroidism.

Interventions

72-hour propanolol before specific treatment of hyperthyroidism

Sponsors

Yaounde Central Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Open label Before and After design

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* consenting patients referred to or diagnosed at the National Centre of Obesity of the Yaounde Central Hospital as having hyperthyroidism * naïve of all treatment specific for hyperthyroidism. * aged 18-70 years

Exclusion criteria

* Patients already under a specific treatment for hyperthyroidism * Patients taking beta blockers or any other cardiospecific treatment * Patients presenting complications including acute thyrotoxic crisis, or symptomatic cardiac failure * Contraindications to the prescription of beta blockers

Design outcomes

Primary

MeasureTime frameDescription
Heart rate variability72 hoursSympatho vagal tone measures

Secondary

MeasureTime frameDescription
Heart rate72 hoursHeart rate

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026