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- Essai clinique NCT01647230
Cerebral Oxygenation and Spinal Anaesthesia in Elderly Patients With Hip Fracture
Observational Study of Cerebral Oxygenation and Spinal Anaesthesia in Elderly Patients With Hip Fracture
Aperçu de l'étude
Statut
Les conditions
Description détaillée
Patients aged 70 years old with hip fracture presenting for surgical repair under intrathecal anaesthesia performed with bupivacaine or L bupivacaine (dose 7 - 9 mg). Preoperative haemoglobin and drugs consumption are registered. All patients receive supplemental oxygen during surgery. Cerebral oximetry, blood pressure, heart rate and oxygen arterial saturation are measured. Level and duration of sensory and motor block are registered. The study observes if there is any correlation between cerebral oximetry and these hemodynamic parameters.
The investigators also observe if there is any correlation between cerebral oximetry and cognitive function evaluated pre and postoperatively by SPMSQ test.
Postoperative SPMSQ test will be performed on the 5th postoperative day and the complications registered.Patients will be followed for the duration of acute hospital stay.
Type d'étude
Inscription (Anticipé)
Contacts et emplacements
Lieux d'étude
-
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Sabadell
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Barcelona, Sabadell, Espagne, 08208
- Recrutement
- Hospital de Sabadell - CSPT
-
Contact:
- Diana L Fernández Galinski, PhD
- Numéro de téléphone: 21277 0034937231010
- E-mail: DFernandez@tauli.cat
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Contact:
- Francisca Gordo Lacal, Dr
- Numéro de téléphone: 21277 0034937231010
- E-mail: fgordo@tauli.cat
-
Chercheur principal:
- Diana L Fernández Galinski, PhD
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion criteria:
- Patients aged >70 years old with hip fracture.
- No contraindication for spinal anaesthesia.
Exclusion Criteria:
- Allergic reaction to local anesthetics.
- Severe aortic stenosis.
- Local infection.
- SPMSQ test >7 errors.
- Patient refusal
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Cerebral Oximetry
Délai: Initial, 3 times after spinal block and every 10 minutes during surgery
|
Changes in cerebral oxymetry measured initially (basal), 10, 20 and 30 minutes after spinal block.
During surgery oximetry is measured evey 10 minutes to obtain the mean of all the values.
|
Initial, 3 times after spinal block and every 10 minutes during surgery
|
|
Mean Arterial Pressure (MAP)
Délai: Initial, 3 times after spinal block and every 10 minutes during surgery
|
Changes in MAP measured initially (basal), 10, 20 and 30 minutes after spinal block.
During surgery oximetry is measured every 10 minutes to obtain the mean of all the values
|
Initial, 3 times after spinal block and every 10 minutes during surgery
|
|
Heart Rate (HR)
Délai: Initial, 3 times after spinal block and every 10 minutes during surgery
|
Changes in HR (basal), 10, 20 and 30 minutes after spinal block.
During surgery oximetry is measured every 10 minutes to obtain the mean of all the values.
|
Initial, 3 times after spinal block and every 10 minutes during surgery
|
|
Oxygen arterial saturation (OSat)
Délai: Initial, 3 times after spinal block and every 10 minutes during surgery
|
Changes in OSat measured initially (basal), 10, 20 and 30 minutes after spinal block.
During surgery oximetry is measured every 10 minutes to obtain the mean of all the values.
|
Initial, 3 times after spinal block and every 10 minutes during surgery
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Short Portable Mental Status Questionnaire (SPMSQ)
Délai: Once before surgery and at 5th postoperative day
|
This test measures cognitive impairment before and after surgery
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Once before surgery and at 5th postoperative day
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Diana L Fernández Galinski, PhD, Hospital de Sabadell - CSPT
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement de l'étude (Anticipé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 2011612CSPT
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