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Comparison of Phenylephrine and Ephedrine in the Treatment of Hemodynamic Disorders After Spinal Anesthesia in the Elderly

Comparison of Phenylephrine and Ephedrine in the Treatment of Hemodynamic Disorders After Spinal Anesthesia in the Elderly

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03858465
Acronym
HypoGer
Enrollment
50
Registered
2019-02-28
Start date
2019-02-01
Completion date
2023-02-01
Last updated
2023-02-24

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

Conditions

Elderly Patients, Hip Fractures, Lower Limb Surgery, Spinal Anesthesia

Keywords

Hypotension, Phenylephrine, Ephedryne

Brief summary

Spinal anesthesia is often used for lower limb surgery in elderly. Hypotension is a side effect of spinal block. In this study, intravenous ephedrine and phenylephrine will be compared with each other to prevent spinal anesthesia-induced hypotension, which is defined in absolute terms as a systolic blood pressure \< 100 mmHg or in relative terms as a 20% fall of systolic blood pressure from baseline.

Detailed description

Randomized single centre clinical randomized study will be performed on 50 participants. The inclusion criteria are participants (age more than 65 years) with proximal femoral fracture scheduled for lower limb surgery under spinal anesthesia. The Ethics Committee approved this prospective study. Informed consent will be taken from individual subjects. Participants are randomly allocated into one of the two study groups. Group A: participants who will receive intravenous 25 mg of ephedrine added to syringe with 50 ml 0,9% sodium chloride solution during 20 minutes. Group B: Phenylephrine 5 mg will be added to syringe with 50 ml 0,9% sodium chloride solution, participants will receive intravenous 0,3 mg of phenylephrine during 20 minutes. Randomization is achieved with the help of Random.org. In order to reduce pain prior to spinal anesthesia an ultrasound-guided fascia iliaca block will be performed using a volume of 30 ml ropivacaine 0,2%. After skin infiltration with 3 ml of lidocaine, a 25G Pencan spinal needle will be inserted at the L3-L4 or L4-L5 vertebral interspaces. After aspirating cerebrospinal fluid, participants will receive hyperbaric bupivacaine 0.5% at 0,11 mg/cm according to the participant height. Ephedrine and phenylephrine will be given intravenous immediately after injection of bupivacaine. Impedance cardiography will be used to measure hemodynamic parameters: cardiac output, stroke volume, cardiac index, stroke index, systemic vascular resistance, systemic vascular resistance index. Heart rate, blood pressure and oxygen saturation will also be controlled. All these parameters will be measured and recorded every 5 minutes until 30 minutes after spinal anesthesia. The data will be statistically analyzed.

Interventions

DRUGEphedrine

intravenous 25 mg of ephedrine

DRUGPhenylephrine

intravenous 0,3 mg of phenylephrine

Sponsors

Medical University of Warsaw
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* elderly (age more than 65 years) * hip fracture scheduled for lower limb surgery under spinal anesthesia * spinal anesthesia

Exclusion criteria

* contraindications to spinal anesthesia * participant refusal * age less than 65 * bradycardia (heart rate less than 60) * participants unable to give consent or inability to communicate

Design outcomes

Primary

MeasureTime frameDescription
blood preasure (mean arterial pressure, systolic and diastolic blood pressure)30 minparameter will be measured and recorded every 5 min after spinal anesthesia.

Secondary

MeasureTime frameDescription
cardiac output, expressed in L/min30 minparameter will be measured using impedance cardiography and recorded every 5 min after spinal anesthesia.
stroke volume, expressed in ml30 minparameter will be measured using impedance cardiography and recorded every 5 min after spinal anesthesia.
cardiac index, expressed in L/min/m2, is the ratio of cardiac output to the body surface area.30 minparameter will be measured using impedance cardiography and recorded every 5 min after spinal anesthesia.
stroke index, expressed in ml/m2, is the ratio of stroke volume to the body surface area.30 minparameter will be measured using impedance cardiography and recorded every 5 min after spinal anesthesia.
heart rate, expressed in bpm30 minparameter will be measured using impedance cardiography and recorded every 5 min after spinal anesthesia.
systemic vascular resistance index, expressed in Dynes.sec.cm-⁵/m2, is the ratio of systemic vascular resistance to the body surface area.30 minparameter will be measured using impedance cardiography and recorded every 5 min after spinal anesthesia.
stroke volume variation, expressed in percentage (%)30 minparameter will be measured using impedance cardiography and recorded every 5 min after spinal anesthesia.
systemic oxygen delivery, expressed in ml/min30 minparameter will be measured using impedance cardiography and recorded every 5 min after spinal anesthesia.
oxygen saturation, expressed in percentage (%)30 minparameter will be measured using pulse oximetry and recorded every 5 min after spinal anesthesia.
systemic vascular resistance, expressed in Dynes.sec.cm-⁵30 minparameter will be measured using impedance cardiography and recorded every 5 min after spinal anesthesia.

Countries

Poland

Outcome results

None listed

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