Acetated Ringer´s Solution in Experimental Hypovolemia

Last updated: March 2, 2024
Sponsor: Oslo University Hospital
Overall Status: Active - Recruiting

Phase

4

Condition

Low Blood Pressure (Hypotension)

Treatment

Lower body negative pressure

Ringer acetate

Clinical Study ID

NCT05705115
Volu-Flow
  • Ages 18-40
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Intravenous fluids are often given to increase stroke volume and thereby improve global oxygen delivery. The effect is however often transient, but the effect of a fluid bolus on stroke volume and other hemodynamic variables over time are poorly described. The volume effect of a fluid bolus (effect on blood volume) can be calculated by measuring Haemoglobin. The purpose of this study is to elucidate the hemodynamic effects of a fluid bolus during normovolemia and hypovolemia in healthy volunteers. Study details include:

• Study Duration: 2 visits of approximately 2 h duration each + follow-up visit. Visits 1 and 2 are at least 2 days apart. Number of Participants: A maximum of 15 participants will be enrolled to study intervention such that 12 evaluable participants complete the study

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Participants who are overtly healthy as determined by medical evaluation includingmedical history, physical examination and focused cardiac ultrasound
  • Capable of giving signed informed consent which includes compliance with therequirements and restrictions listed in the informed consent form (ICF) and in thisprotocol
  • Sex and Contraceptive/Barrier Requirements Male participants: Not applicable. Femaleparticipants: Use of adequate birth control for women of childbearing potential.
  • A woman is considered of childbearing potential (WOCBP), i.e. fertile, followingmenarche and until becoming post-menopausal unless permanently sterile when sexuallyactive. Permanent sterilisation methods include hysterectomy, bilateral salpingectomyand bilateral oophorectomy. A postmenopausal state is defined as no menses for 12months without an alternative medical cause. A high follicle stimulating hormone (FSH)level in the postmenopausal range may be used to confirm a post-menopausal state inwomen not using hormonal contraception or hormonal replacement therapy. However, inthe absence of 12 months of amenorrhea, a single FSH measurement is insufficient.
  • Inclusion of WOCBP is possible when either:
  • Using at least an acceptable effective contraceptive measure (combined (estrogen andprogestogen containing) hormonal contraception, progestogen-only hormonalcontraception associated with inhibition of ovulation, intrauterine device,intrauterine hormone-releasing system, bilateral tubal occlusion, vasectomised partneror sexual abstinence). As a minimum contraception should be maintained until treatmentdiscontinuation. or
  • Confirmed negative highly sensitive urine or serum pregnancy test at screening. Apregnancy test is performed at any visit before administering IMP if more than 14 dayshave passed since last pregnancy test. There will be no demand for post-interventioncontraception.

Exclusion

Exclusion Criteria: Participants are excluded from the study if any of the following criteria apply: Medical Conditions

  1. Any medical condition limiting physical exertional capacity or requiring regularmedication (allergy and contraceptives excepted).
  2. Pregnancy.
  3. Breastfeeding.
  4. History of syncope (syncope of presumed vasovagal nature with known precipitatingfactor excepted).
  5. Any known cardiac arrhythmia. Prior/Concomitant Therapy
  6. Any drug (contraceptives excepted) used on a regular basis for a chronic condition (allergy excepted).

Study Design

Total Participants: 12
Treatment Group(s): 2
Primary Treatment: Lower body negative pressure
Phase: 4
Study Start date:
March 02, 2024
Estimated Completion Date:
July 29, 2024

Study Description

Administration of intravenous fluids is one of the most commonly performed procedures in anaesthesia, critical care and emergency medicine. Intravenous fluids can be given to achieve specific goals depending on the type of fluid, but often, fluid is given simply to expand the intravascular volume. The volume-expanding effect of intravenous fluids is however time-dependent, and often of limited duration as fluid is distributed out of the intravascular space and eliminated mainly in the kidneys.

The goal of intravascular volume expansion is to improve haemodynamic variables, such as SV, CO and ABP. The reasoning is that volume expansion increases SV mainly mediated by the Frank-Starling mechanism. The degree to which SV increases with volume expansion is termed fluid responsiveness.1 The increase in SV does however in most cases seem to be transient. The reason for the transient nature of the hemodynamic response is not known, but may be related to reduction in intravascular volume expansion as described above or other factors, such as vasodilation.

Calculation of volume expansion:

The volume-expanding effect of intravenous fluids has been studied by measuring concentration of hemoglobin. Under the assumption that hemoglobin is evenly distributed in, and does not leave the intravascular space, intravascular volume can be calculated and kinetic studies of the volume effect (volume kinetics) can be performed.

Hb = intravascular amount of hemoglobin V0 = Intravascular volume at time 0 Vt = Intravascular volume at time t [Hb]0 = Hemoglobin concentration at time 0 [Hb]t = Hemoglobin concentration at time t Eq1: (Hb)o= Hb/Vo. Vo = Hb/(Hb)o Eq 2: (Hb)t= Hb/Vt. Vo = Hb/(Hb)t.

Assuming that the amount of hemoglobin is constant, from Eq 1 ang Eq 2, it follows that:

Eq 3: Vt/V0=(Hb)o/(Hb)t which therefore gives the relative value of intravascular volume at time=t to compared to time=0; Vt_rel.

Kinetic model of outcomes:

Similar to the volume expansion, the relative value of the hemodynamic variables compared to baseline can be calculated, expressed as value at time=t, Vt.

A pharmacokinetic model can then be fitted to the observations. In a two-compartment model, the relative value (e.g. volume) of the observed value at time=t (Vt) can be described as:

Eq 4: V_(t_rel)=D(〖Ae〗^(-αt)+〖Be〗^(-βt))

A one-compartment model can be described as:

Eq 5: V_(t_rel)=D(〖Ae〗^(-αt)) A two-compartment model will typically describe a rapid equilibration with one compartment and a slower elimination. Initially the reduction in Vt is dominated by distribution, and later by the slower elimination. Each of these effects have their own half-lives, given by α and β. For a one-compartment model, the reduction in Vt is best described by a single half-life.

LBNP-model:

LBNP is a model that has been used for several decades. Lower body negative pressure (LBNP) is a model of central hypovolemia where negative pressure is applied to the body from the waist-down. Thereby, blood is displaced from the central compartment of the upper body to the lower extremities and pelvis. The model has been used for more than half a century and is considered useful model for studying hypovolemia in conscious volunteers.

The volume kinetics of intravenous fluids has been shown to be affected by volume status, with a longer lasting volume effect during hypovolaemia.The effects of volume status on the hemodynamic response to intravenous fluids has been less explored.

Aim of the study The aim of the present study is to explore the effects over time of an intravenous fluid bolus. The effects on the volume expanding effects and the hemodynamic effects will be measured.

Connect with a study center

  • Oslo University Hospital

    Oslo, 0586
    Norway

    Active - Recruiting

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