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Effects of IV Administration of Ketamine on the Analgesia Nociception Index (ANI) Measured With the PhysioDoloris

24 de junio de 2019 actualizado por: Laurent Bollag, University of Washington

The Effects of Intravenous Administration of Ketamine on the Analgesia Nociception Index (ANI) Measured With the PhysioDoloris Device

This study evaluates effects of the analgesic ketamine on ANI measurements (Anti Nociceptive Index)

Descripción general del estudio

Estado

Terminado

Condiciones

Descripción detallada

Researchers at the University of Washington are doing this study to find out if a commonly used anesthetic affects patients Analgesia Nociception Index (level of pain relief) during abdominal hysterectomy under general anesthesia.

The investigators will administer routine anesthesia care including Ketamine, a commonly used anesthetic, during the patients surgery. During the patients surgery, the investigators will monitor the patients level of pain relief using the PhysioDoloris monitor, which monitors the routinely used EKG monitor. Though not yet FDA approved, the PhysioDoloris is completely non-invasive and collects data from the EKG monitor.

Tipo de estudio

De observación

Inscripción (Actual)

20

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

  • Estados Unidos
    • Washington
      • Seattle, Washington, Estados Unidos, 98195
        • University of Washington

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Femenino

Método de muestreo

Muestra no probabilística

Población de estudio

Women undergoing gynecological/abdominal surgery

Descripción

Inclusion Criteria:

  • ASA status I, II, or III
  • 18 years or older
  • Receiving GA with uncomplicated routine intubation
  • Ability to provide informed consent
  • English-speaking

Exclusion Criteria:

  • Presence of coronary artery disease, cardiac arrhythmias, or ketamine allergy
  • Patient refusal
  • History of substance abuse
  • Patients taking psychotropic and/or opiate drugs
  • Having a history of psychiatric diseases or psychological problems

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Mean ANI Changes After Intubation
Periodo de tiempo: Before vs after intubation
ANI stands for Analgesia Nociception Index. Its a dimension less number computed by a pain monitor ranging from 0-100. An index of 100 means absent pain, and the number decreases as pain increases. ANI was measured pre- and post- Intubation
Before vs after intubation
Mean ANI Changes 3 Min After Ketamine Bolus
Periodo de tiempo: Before vs 3 min after Ketamine adminstration
ANI was measured pre- and post- i.v. ketamine administration
Before vs 3 min after Ketamine adminstration
Mean ANI Changes 5 Min After Ketamine Bolus
Periodo de tiempo: Before vs 5 min after Ketamine adminstration
ANI was measured pre- and post- i.v. ketamine administration
Before vs 5 min after Ketamine adminstration
Mean ANI Changes After Skin Incision
Periodo de tiempo: Before vs after skin incision
ANI was measured pre- and post- skin incision
Before vs after skin incision

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Mean BIS Changes After Intubation
Periodo de tiempo: Before vs after intubation

BIS was measured pre- and post-intubation.

BIS, Bispectral index, is an indication of anesthesia depth and measured by a monitor during surgery (0-100 scale, range described below). Depth of sedation is calculated by measuring cerebral electric activity via an electroencephalogram (EEG).

  • 100-90: awake and responding appropriately to verbal stimulation
  • 80-70: responsive to loud commands or mild shaking
  • 60-40: unresponsive to verbal stimulus; general anesthesia obtained with a low chance for explicit recall
  • <40: deep hypnotic state; possible protective responses still intact
  • <20: burst suppression (EEG pattern characterized by cycles of high-voltage electrical movement alternating with cycles of no activity in the brain); respiratory drive is limited, but possible protective responses still intact
  • 0: totally suppressed EEG (flat line)
Before vs after intubation
Mean BIS Changes 3 Min After Ketamine Bolus
Periodo de tiempo: Before vs 3 min after Ketamine adminstration

BIS was measured pre- and post-Ketamine administration.

BIS, Bispectral index, is an indication of anesthesia depth and measured by a monitor during surgery (0-100 scale, range described below). Depth of sedation is calculated by measuring cerebral electric activity via an electroencephalogram (EEG).

  • 100-90: awake and responding appropriately to verbal stimulation
  • 80-70: responsive to loud commands or mild shaking
  • 60-40: unresponsive to verbal stimulus; general anesthesia obtained with a low chance for explicit recall
  • <40: deep hypnotic state; possible protective responses still intact
  • <20: burst suppression (EEG pattern characterized by cycles of high-voltage electrical movement alternating with cycles of no activity in the brain); respiratory drive is limited, but possible protective responses still intact
  • 0: totally suppressed EEG (flat line)
Before vs 3 min after Ketamine adminstration
Mean BIS Changes After Skin Incision
Periodo de tiempo: Before vs after skin incision

BIS was measured pre- and post-skin incision.

BIS, Bispectral index, is an indication of anesthesia depth and measured by a monitor during surgery (0-100 scale, range described below). Depth of sedation is calculated by measuring cerebral electric activity via an electroencephalogram (EEG).

  • 100-90: awake and responding appropriately to verbal stimulation
  • 80-70: responsive to loud commands or mild shaking
  • 60-40: unresponsive to verbal stimulus; general anesthesia obtained with a low chance for explicit recall
  • <40: deep hypnotic state; possible protective responses still intact
  • <20: burst suppression (EEG pattern characterized by cycles of high-voltage electrical movement alternating with cycles of no activity in the brain); respiratory drive is limited, but possible protective responses still intact
  • 0: totally suppressed EEG (flat line)
Before vs after skin incision
Mean Heart Rate Change After Intubation
Periodo de tiempo: Before vs after intubation
Heart rate assessed by continuous pulse oximetry. Heart rate was measured pre- and post-intubation.
Before vs after intubation
Mean Heart Rate Change 3 Min After Ketamine Bolus
Periodo de tiempo: Before vs 3 min after Ketamine adminstration
Heart rate was measured pre- and post- Ketamine administration
Before vs 3 min after Ketamine adminstration
Mean Heart Rate Change After Skin Incision
Periodo de tiempo: Before vs after skin incision
Heart rate was measured pre- and post-skin incision.
Before vs after skin incision
Change in Mean Arterial Pressure After Intubation
Periodo de tiempo: Before vs after intubation
MAP or mean arterial pressure is the average blood pressure of an individual and is measured non-invasively during surgery. MAP was measured pre- and post-intubation.
Before vs after intubation
Change in Mean Arterial Pressure After 3 Min After Ketamine Bolus
Periodo de tiempo: Before vs 3 min after Ketamine adminstration
MAP was measured pre- and post-ketamine administration
Before vs 3 min after Ketamine adminstration
Mean MAP Changes After Skin Incision
Periodo de tiempo: Before vs after skin incision
MAP was measured pre- and post- skin incision.
Before vs after skin incision

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Average Ketamine Used
Periodo de tiempo: Surgery
Amount of Ketamine used during surgery
Surgery

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

University of Washington

Investigadores

  • Investigador principal: Laurent Bollag, MD, University of Washington

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de agosto de 2012

Finalización primaria (Actual)

1 de diciembre de 2012

Finalización del estudio (Actual)

1 de diciembre de 2012

Fechas de registro del estudio

Enviado por primera vez

10 de octubre de 2012

Primero enviado que cumplió con los criterios de control de calidad

25 de octubre de 2012

Publicado por primera vez (Estimar)

30 de octubre de 2012

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

5 de agosto de 2019

Última actualización enviada que cumplió con los criterios de control de calidad

24 de junio de 2019

Última verificación

1 de junio de 2019

Más información

Términos relacionados con este estudio

Palabras clave

Otros números de identificación del estudio

  • 42398

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

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