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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05713396
Other study ID # 72405
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date January 1, 2017
Est. completion date June 1, 2022

Study information

Verified date January 2023
Source AHEPA University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose: To investigate the effect of Quinapril (Q) or Losartan (L) or their combination on definite Diabetic Autonomic Neuropathy (DAN) and left ventricular systolic and diastolic function (LVF) over a period of 4 years. Patients-methods: Fifty-nine patients with definite DAN [2 or more of the 4 Cardiovascular Reflex Tests (CRTs) were abnormal] were studied for 4 years. Patients were randomly allocated in 3 groups receiving A, 20 mg Q, B, 100 mg L and C, 20 mg Q +100 mg L respectively. CRTs analyzed with Mean Circular Resultant (MCR), Valsalva index, 30:15 ratio and postural hypotension. LV function was investigated with radionuclide ventriculography (RNV) at rest. Ejection fraction was used to assess LV systolic function, while peak filling rate, first third filling fraction, and atrial contribution to ventricular filling were used to investigate LV diastolic function. CRTs and RNV were performed at baseline and after 4 years.


Recruitment information / eligibility

Status Completed
Enrollment 59
Est. completion date June 1, 2022
Est. primary completion date June 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. >18 years old 2. Diabetes mellitus 3. Diabetic autonomic neuropathy Exclusion Criteria: 1. Coronary artery disease 2. Arterial hypertension 3. Heart failure with reduced ejection fraction LVEF<40% 4. Any contraindication to undergo radionuclide ventriculography

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Quinapril
Per os
Losartan
Per os
Quinapril + Losartan
Per os

Locations

Country Name City State
Greece Diabetes Center, 1st Propeudetic Department of Internal Medicine, Medical School, Aristotle University of Thessaloniki, "AHEPA'' Hospital Thessaloníki

Sponsors (1)

Lead Sponsor Collaborator
AHEPA University Hospital

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary MCR Mean Circular Resultant 4 years
Primary AV Atrial contribution to ventricular filling 4 years
Secondary E/I Index Expiration/Inspiration Index 4 years
Secondary SD Standard Deviation 4 years
Secondary Valsalva Index Valsalva Maneuver 4 years
Secondary 30:15 Index Variation of R-R interval during postural change 4 years
Secondary Postural hypotension Variation of systolic blood pressure during postural change (standing) 4 years
Secondary EF Left ventricular ejection fraction 4 years
Secondary PER Peak emptying rate 4 years
Secondary PFR Peak filling rate Peak filling rate 4 years
Secondary 1/3 FF Filling fraction during the first third of the diastole 4 years
Secondary TPF/FT Time to peak filling time/filling time 4 years
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