Levalbuterol Compared to Albuterol Regarding Cardiac Side Effects and Potassium Lowering Effects.
Primary Purpose
Hyperkalemia
Status
Recruiting
Phase
Phase 4
Locations
Syrian Arab Republic
Study Type
Interventional
Intervention
Levalbuterol
Albuterol
Sponsored by
About this trial
This is an interventional treatment trial for Hyperkalemia focused on measuring Hyperkalemia, Albuterol, Levalbuterol, Heart rate
Eligibility Criteria
Inclusion Criteria:
- adult patients
- serum potassium level >5.9 mEq/L
Exclusion Criteria:
Pseudohyperkalemia:
- Hemolysis of blood sample
- Thrombocytosis > 10*6 /mm3
- Hyperleukocytosis > 10*5/mm3
- Mechanical Trauma during Venipuncture
- Fist clenching during blood drawing
- Tourniquet time > 1 minute
Diabetes acute complications
- DKA
- Hyperosmolar Hyperglycemic Syndrome
- Insulin-dependent diabetes mellitus ( if insulin is taken recently)
- Pregnant women
- Hyperthyroidism
- Hemodynamic instability
- Pacemakers if providing impulses (demand pacemakers that are not firing right now are included)
- Atrial fibrillation or any other arrhythmia
- Baseline tachycardia >120 bpm
- Acute exacerbations of HF
- Patients expected to require emergency intubation and ventilation
- Patients expected to require dialysis within the first 60 minutes
- Patients with hypersensitivity to the medication
- Patients with Acute Coronary Syndrome
- Patients on beta-blockers / beta-agonists or anti-arrhythmic drugs
- Patients with severe dyspnea or hypoxia SpO2 <90%
Sites / Locations
- Aleppo University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Levalbuterol Arm
Albuterol Arm
Arm Description
Outcomes
Primary Outcome Measures
Heart rate changes
Heart rate changes over time measured as beats per minute
Serum potassium level changes
Serum potassium level changes after treatment measured as mEq/L
Secondary Outcome Measures
ECG changes
ECG Changes at presentation with hyperkalemia (Depressed ST segment, Diphasic T wave, Prominent U wave, Peaked T wave, Wide PR interval, Wide QRS duration, Peaked T wave, Loss of P wave, Sinusoidal wave, Others) and after treatment
Blood Pressure (BP) changes
BP changes over time measured as mmHg
Frequency of reported symptoms at presentation
Symptoms at presentation (Muscle weakness, Paresthesia, Paralysis, flushing, Nausea/Vomiting, Chest pain, Dyspnea, Fasciculation, Palpitations, Others).
Frequency of Adverse effects
Adverse effects following treatment (Fever, Palpitations, Hypoglycemia, Hypokalemia, Headache, Tremor, Nervousness, Nausea/vomiting, Lightheadedness)
Full Information
NCT ID
NCT05173584
First Posted
November 24, 2021
Last Updated
December 12, 2021
Sponsor
University of Aleppo
1. Study Identification
Unique Protocol Identification Number
NCT05173584
Brief Title
Levalbuterol Compared to Albuterol Regarding Cardiac Side Effects and Potassium Lowering Effects.
Official Title
Is Levalbuterol an Effective Treatment With Less Cardiac Side Effects Than Albuterol in Hyperkalemia Patients: A Randomized-controlled Clinical Trial Protocol.
Study Type
Interventional
2. Study Status
Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
November 4, 2021 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Aleppo
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Hyperkalemia is a common life-threatening electrolyte disturbance which may impair cardiac and many other organs' functions. Unfortunately, a well-established guideline for the treatment of hyperkalemia in the emergency setting is still missing. However, the last "Kidney Disease: Improving Global Outcomes (KDIGO)" conference proposed a treatment protocol for hyperkalemia and addressed controversies in this matter. Beta2-agonists were one of the main lines in the approach towards managing a patient with hyperkalemia. However, this evidence was only available for racemic albuterol.
Levalbuterol is the isolated R-enantiomer of racemic albuterol which is comprised of S- and R-enantiomers. Several lab and clinical studies have assessed the effect, affinity, and selectivity of each of the enantiomers. Few studies in medical literature have compared the difference between these two drugs regarding cardiac effects with inconclusive results, and even fewer studies have compared the efficacies of these two drugs regarding potassium lowering effect.
To the investigators' knowledge, no study to date has compared the efficacy and safety of albuterol compared to levalbuterol in hyperkalemic patients with the properly adjusted dosing. So, in clinical practice, the investigators wanted to know based on evidence if levalbuterol can be an effective substitute for albuterol in lowering potassium levels in hyperkalemia patients while yielding fewer cardiac side effects. To answer this question, the investigators designed a single-centered controlled clinical trial that includes adult hyperkalemia patients in Aleppo University Hospital.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperkalemia
Keywords
Hyperkalemia, Albuterol, Levalbuterol, Heart rate
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Levalbuterol Arm
Arm Type
Experimental
Arm Title
Albuterol Arm
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Levalbuterol
Intervention Description
Levalbuterol nebulizer solution 1.25mg/3ml with a total dose of 5 mg (12ml) for each patient.
Intervention Type
Drug
Intervention Name(s)
Albuterol
Other Intervention Name(s)
salbutamol, racemic albuterol
Intervention Description
Albuterol nebulizer solution 2.5 mg/3ml with a total dose of 0 mg (12ml) for each patient.
Primary Outcome Measure Information:
Title
Heart rate changes
Description
Heart rate changes over time measured as beats per minute
Time Frame
Heart rate is measured at baseline before drug administration and at 15, 30, 45, 60, 90, 120 minutes after treatment.
Title
Serum potassium level changes
Description
Serum potassium level changes after treatment measured as mEq/L
Time Frame
Serum potassium levels are measured at baseline and 90 minutes after treatment administration
Secondary Outcome Measure Information:
Title
ECG changes
Description
ECG Changes at presentation with hyperkalemia (Depressed ST segment, Diphasic T wave, Prominent U wave, Peaked T wave, Wide PR interval, Wide QRS duration, Peaked T wave, Loss of P wave, Sinusoidal wave, Others) and after treatment
Time Frame
ECG changes detected at baseline and at 90 minutes after therapy
Title
Blood Pressure (BP) changes
Description
BP changes over time measured as mmHg
Time Frame
BP changes measured at baseline and at 30, 60, and 90 minutes after therapy
Title
Frequency of reported symptoms at presentation
Description
Symptoms at presentation (Muscle weakness, Paresthesia, Paralysis, flushing, Nausea/Vomiting, Chest pain, Dyspnea, Fasciculation, Palpitations, Others).
Time Frame
Symptoms reported only at the presentation of the patient
Title
Frequency of Adverse effects
Description
Adverse effects following treatment (Fever, Palpitations, Hypoglycemia, Hypokalemia, Headache, Tremor, Nervousness, Nausea/vomiting, Lightheadedness)
Time Frame
Adverse effects after treatment detected during the first two hours following treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
adult patients
serum potassium level >5.9 mEq/L
Exclusion Criteria:
Pseudohyperkalemia:
Hemolysis of blood sample
Thrombocytosis > 10*6 /mm3
Hyperleukocytosis > 10*5/mm3
Mechanical Trauma during Venipuncture
Fist clenching during blood drawing
Tourniquet time > 1 minute
Diabetes acute complications
DKA
Hyperosmolar Hyperglycemic Syndrome
Insulin-dependent diabetes mellitus ( if insulin is taken recently)
Pregnant women
Hyperthyroidism
Hemodynamic instability
Pacemakers if providing impulses (demand pacemakers that are not firing right now are included)
Atrial fibrillation or any other arrhythmia
Baseline tachycardia >120 bpm
Acute exacerbations of HF
Patients expected to require emergency intubation and ventilation
Patients expected to require dialysis within the first 60 minutes
Patients with hypersensitivity to the medication
Patients with Acute Coronary Syndrome
Patients on beta-blockers / beta-agonists or anti-arrhythmic drugs
Patients with severe dyspnea or hypoxia SpO2 <90%
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Baraa Shebli, M.D.
Phone
+963949938945
Email
bshebli@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Mike Ghabally, M.D.
Phone
+963993856840
Email
mike.ghabally@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mahmoud Malhis, MRCP
Organizational Affiliation
Professor of Cardiology, Head of Cardiology division, Aleppo University Hospital, Faculty of Medicine, University of Aleppo.
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Baraa Shebli, M.D.
Organizational Affiliation
Cardiology Resident, Aleppo University Hospital, Faculty of Medicine, University of Aleppo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aleppo University Hospital
City
Aleppo
State/Province
Aleppo Provice
ZIP/Postal Code
22743
Country
Syrian Arab Republic
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rima Alassaf
Email
admin@auh.edu.sy
First Name & Middle Initial & Last Name & Degree
Mike Ghabally, M.D.
First Name & Middle Initial & Last Name & Degree
Hamed Kozom, M.D.
First Name & Middle Initial & Last Name & Degree
Muhammad Besher Shabouk, Undergraduate
12. IPD Sharing Statement
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Levalbuterol Compared to Albuterol Regarding Cardiac Side Effects and Potassium Lowering Effects.
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