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A Dose Response Trial Using 5 and 10 Mg of Midodrine Hydrochloride

A Dose Response Trial Using 5 and 10 mg. of Midodrine Hydrochloride to Treat Orthostatic Hypotension in Persons With SCI

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00426842
Enrollment
11
Registered
2007-01-25
Start date
2007-01-31
Completion date
2011-03-31
Last updated
2016-10-10

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

Conditions

Orthostatic Hypotension, Spinal Cord Injury

Keywords

Blood pressure, Orthostatic hypotension, Spinal Cord Injury, Sympathetic vascular control, Midodrine

Brief summary

With upright postures, there is an immediate redistribution of blood to the dependent circulation; venous return and central venous filling pressure are reduced, resulting in diminution of cardiac output and blood pressure. These hemodynamic alterations stimulate the baroreceptor reflex, which is mediated via the central nervous system to increase peripheral sympathetic vasomotor tone, restoring blood pressure and cardiac output within seconds-to-minutes of the assumption of the upright position. Following SCI, individuals often experience the inability to adjust to postural changes due to disruption of central command of the baroreceptor reflex and reduction in efferent sympathetic neural pathways; consequently, orthostatic hypotension (OH) and symptoms of cerebral hypo-perfusion may ensue. OH is a well-documented phenomenon, which is characterized by a fall in systolic blood pressure of \>20 mmHg or diastolic BP of \> 10 mmHg within 3 minutes of assumption of an upright posture. As a consequence of OH, many individuals experience symptoms of cerebral hypo-perfusion which include lightheadedness, dizziness, blurry vision, fatigue, nausea, ringing in the ears, cognitive impairment and heart palpitations. Although several investigators have reported increased prevalence of OH during the acute phase of spinal cord injury (SCI), individuals with chronic injury also experience significant falls in blood pressure with seated upright postures. This investigation will examine the effects of an alpha-agonist, midodrine hydrochloride, during head-up tilt on systemic blood pressure, cerebral blood flow and cerebral oxygenation compared to placebo administration in persons with chronic SCI who demonstrate significant orthostatic hypotension during a 24-hour observation study. This is the first study to determine the dose response and efficacy of midodrine to improve orthostatic blood pressure and cerebral blood flow and oxygenation in the SCI population.

Detailed description

In individuals with SCI, blood pressure regulation is altered compared to the non-SCI population and relates to the degree of sympathetic vascular denervation. The inadequate release of norepinephrine with postural change is a primary component of OH and several reports have documented significantly reduced plasma norepinephrine levels in individuals with tetraplegia. Ephedrine sulfate and midodrine hydrochloride, both 1 receptor agonists, are recommended for the treatment of postural hypotension in this population. Although there are case reports documenting improved blood pressure regulation in persons with SCI treated with an 1 receptor agonist, this pharmacological treatment for OH has not been adequately studied in this population. A dose response trial will be used to determine the efficacy of midodrine hydrochloride (5 and 10 mg) compared to no drug at improving systemic blood pressure, cerebral blood flow and oxygenation and at reducing symptomatic hypotension during tilt-table testing in 16 individuals with SCI who manifest significant orthostatic hypotension (total time \[minutes\] spent with hypotension \[ 20% fall in mean arterial pressure from supine laboratory observation\] over a 24-hour observation. Subjects will receive, in an increasing dose manner and on separate days: no drug, 5 and 10 mg of oral midodrine hydrochloride. Oral ingestion of the pill (placebo or midodrine) will be at 30 minutes during the 60 minute supine rest period prior to the head-up tilt maneuver. A progressive head-up tilt will be utilized in which the table will be adjusted to 15 , 25 , 35 for 5 minutes at each angle and then will be maintained at 45 for 45 minutes or until the subjects experiences symptoms of compromised cerebral blood flow, which include, but are not limited to, light headedness, blurry vision, dizziness and nausea. Throughout each test day, measurements of heart rate, blood pressure, middle cerebral blood flow velocity, and cerebral oxygenation will be obtained. In addition, blood draws will be completed to capture humoral factors responsible for blood pressure regulation.

Interventions

Alpha1-agonist, exerts its actions via activation of the alpha-adrenergic receptors of the arteriolar and venous vasculature, producing an increase in vascular tone and elevation of blood pressure.

Sponsors

James J. Peters Veterans Affairs Medical Center
Lead SponsorFED

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* This study will be performed on subjects 18 to 65 years old, with chronic SCI (\> 1 year), who are neurologically stable and have demonstrated significant hypotension (total time \[proportion 50%\] spent with hypotension \[systolic BP below 110 mmHg for males and 100 mmHg for females\] during a 24-hour observation.

Exclusion criteria

* hypertension * diabetes * vascular disease * cardiac disease * cardiovascular medication * pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Systolic Blood PressureThe difference between the average supine systolic blood pressure and the average systolic blood pressure at 45 degree head-up tilt position.brachial artery systolic blood pressure (mmHg)

Countries

United States

Participant flow

Recruitment details

2008-2010

Pre-assignment details

no subject was excluded from study participate prior to group assignment.

Participants by arm

ArmCount
Arm 1
Blood pressure response during HUT following administration of Midodrine Hydrochloride compared with no drug.
11
Total11

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyLost to Follow-up1

Baseline characteristics

CharacteristicArm 1
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
11 Participants
Age, Continuous42 years
STANDARD_DEVIATION 9
Region of Enrollment
United States
11 participants
Sex: Female, Male
Female
2 Participants
Sex: Female, Male
Male
9 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 11
serious
Total, serious adverse events
0 / 11

Outcome results

Primary

Systolic Blood Pressure

brachial artery systolic blood pressure (mmHg)

Time frame: The difference between the average supine systolic blood pressure and the average systolic blood pressure at 45 degree head-up tilt position.

ArmMeasureGroupValue (MEAN)Dispersion
No-drugSystolic Blood PressureBaseline Blood Pressure98 mmHgStandard Deviation 5
No-drugSystolic Blood PressureHead-up Tilt Blood Pressure87 mmHgStandard Deviation 15
Midodrine 5 mgSystolic Blood PressureBaseline Blood Pressure97 mmHgStandard Deviation 5
Midodrine 5 mgSystolic Blood PressureHead-up Tilt Blood Pressure96 mmHgStandard Deviation 19
Midodrine 10 mgSystolic Blood PressureBaseline Blood Pressure102 mmHgStandard Deviation 12
Midodrine 10 mgSystolic Blood PressureHead-up Tilt Blood Pressure109 mmHgStandard Deviation 22

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026