- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01677234
Wrist NIBP During Elective Cesarean Delivery
Comparison of Arm and Forearm Blood Pressure During Elective Cesarean Delivery
Studienübersicht
Status
Detaillierte Beschreibung
Upper arm non-invasive blood pressure (NIBP) measurement is the most commonly accepted method of blood pressure (BP) monitoring. During a cesarean delivery it may be challenging to obtain an accurate measurement from the automated devices in over 50% of the attempts due to arm movement.1 Patients may voluntarily move their arm, but more often neuraxial (spinal, epidural, combined spinal-epidural) anesthesia is known to induce shivering that causes the patient's arm to shake.2 To eliminate the effect of movement of the upper arm, NIBP has been tested on the leg because it is immobilized during neuraxial anesthesia. However, studies monitoring NIBP on an ankle or a calf were unable to accurately detect changes (increase or decrease) in blood pressure in patients undergoing a cesarean delivery.3,4 It seems clinically reasonable that in the case of a shivering patient, the forearm, with less muscle mass, would shake less and could be stabilized more easily than the upper arm (stabilizing the forearm is easily done by holding the patient's hand with a light pressure on the arm rest). Therefore, positioning an NIBP cuff on the forearm (near the wrist) may be useful to obtain an accurate blood pressure measurement in shivering patients.
Previous studies have found that forearm BP overestimates blood pressure measured at the upper arm in a variety of clinical settings and patient populations under static (patient at rest, not submitted to an intervention that might alter BP) circumstances.5-8 It is unknown whether this overestimation is clinically relevant when blood pressure change occurs rapidly, such as during a cesarean delivery. During neuraxial anesthesia for cesarean delivery, it is important for the anesthesiologist to know both absolute values and clinically significant changes in blood pressure to determine their treatment. The detection of dynamic changes in blood pressure (as when the patient is submitted to an intervention that might alter BP per se, e.g. neuraxial anesthesia) has been studied in obstetric patients. Nevertheless, either due to the location where the BP cuff was placed4 (as on the lower limb with interference of the aorto-caval compression) or to the technology used to measure blood pressure,9 (the penaz technology was not consistent with oscillometric technology in a previous study) the forearm blood pressure was not comparable to upper arm blood pressure when measured using an oscillometric monitor.
This study will compare the upper arm (the current gold-standard) and the forearm NIBP measurements in patients undergoing an elective cesarean delivery under subarachnoid anesthesia. We hypothesize that the forearm systolic BP measurement values will be within 10% (lower or higher) of the systolic BP values measured in the upper arm at the same time-points
Studientyp
Einschreibung (Tatsächlich)
Kontakte und Standorte
Studienorte
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British Columbia
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Vancouver, British Columbia, Kanada, V6H 3N1
- British Columbia's Women's Hospital
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Probenahmeverfahren
Studienpopulation
Beschreibung
Inclusion Criteria:
- Healthy (American Society of Anesthesiologist's (ASA) physical status I or II) patients
- Having an elective cesarean delivery under spinal or combined spinal epidural anesthesia
- ≥19 years old
Exclusion Criteria:
- Contra-indication to neuraxial anesthesia
- General anesthesia for any reason prior to delivery of the baby
- Use of the epidural component (epidural top-up) of combined spinal epidural anesthesia (prior to delivery of the baby)
- History of cardiovascular disease, e.g. hypertension (either essential or pregnancy-induced)
- A difference of more than 10% between both upper arms and forearms in mean blood pressure measurement prior to surgery (see below)
- BMI >35kg/m2 (it is more difficult to ensure the cuff size is correct in these obese patients)
- Inability to read and understand English for the purpose of informed consent
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
Kohorten und Interventionen
Gruppe / Kohorte |
|---|
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Pregnant women
Pregnant women undergoing a cesarean section
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Compare trends in NIBP measurements between the upper arm and forearm
Zeitfenster: 30 minutes
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Measure NIBP at the upper arm and forearm simultaneously during surgery.
NIBP cuffs will be on opposite arms.
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30 minutes
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
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To estimate the accuracy of blood pressure measured on the forearm
Zeitfenster: 30 minutes
|
30 minutes
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Simon Massey, MD, University of British Columbia, BC Women's Hospital
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
- H12-01797
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