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Fluid Infusion During Breast Surgery

Només els usuaris registrats poden traduir articles
Inicieu sessió / registreu-vos
L'enllaç es desa al porta-retalls
Estat
Patrocinadors
Rigshospitalet, Denmark

Paraules clau

Resum

The investigators want to investigate the effects of two different kinds of fluid infusions given during varicose vein surgery. Both types of fluid are regularly given during surgery, and the investigators want to compare their respective effects on balance, nausea/vomiting and orthostatic function after surgery.
The investigators' hypothesis is that using a colloid solution will improve orthostatic function, balance, nausea/vomiting and reduce hospital stay.

Descripció

The optimal amount and type of fluid given during surgery has not been defined. It has been agreed that hypovolemia must be avoided, but at the same time it has been agreed that fluid excess is harmful for organ function.When distributing fluids it is usually either crystalloids og colloids which are given. The effects of the two types of fluid have not been compared. Our hypothesis is that using a colloid (HES 130/0,4) will improve orthostatic function, nausea/vomiting and shorten hospital stay, compared to using a crystalloid (Lactated Ringer's solution).The amount of fluid the patient receives, will be individually tailored by monitoring SV using esophageal Doppler technique during surgery.

Dates

Darrera verificació: 01/31/2009
Primer enviat: 02/04/2007
Inscripció estimada enviada: 02/04/2007
Publicat per primera vegada: 02/05/2007
Última actualització enviada: 02/26/2009
Publicació de l'última actualització: 03/02/2009
Data d'inici de l'estudi real: 03/31/2009
Data estimada de finalització primària: 08/31/2009
Data estimada de finalització de l’estudi: 08/31/2009

Condició o malaltia

Breast Surgery

Intervenció / tractament

Drug: Hydroxyethylstarch 130/0,4

Drug: Lactated Ringer's solution

Fase

Fase 4

Criteris d'elegibilitat

Edats elegibles per estudiar 18 Years Per a 18 Years
Sexes elegibles per estudiarAll
Accepta voluntaris saludables
Criteris

Inclusion Criteria:

- Patients having performed elective breast surgery.

- Age between 18 and 70 years

- Patients who have given written consent to participate in the project after haven completely understood the contents and limitations of the protocol.

Exclusion Criteria:

- Patients who do not understand or speak Danish

- Patients who have not signed the informed consent or the written authority

- pre-medication, except 1g paracetamol

- ASA > II

- Pregnant or breastfeeding

- Known to have Renal disease

- Known to have Psychiatric disorder (not considering the use of SSRI antidepressive)

- Need for crash induction or prone position.

- Oesophageal varicoses

- Necrosis or cancer in: Mouth, Pharynx, Larynx or Oesophagus

- Coarctation or aneurism in the proximal Aorta

- Severe bleeding disease

Resultat

Mesures de resultats primaris

1. To investigate orthostatic function, measured by Finapress [undefined]

Mesures de resultats secundaris

1. To investigate the occurrence of postsurgery nausea/vomiting. [undefined]

2. To investigate the amount of time until discharge criteria from the Postanaesthetic Care Unit have been achieved. [undefined]

3. To investigate balance function, measured by BalanceMaster [undefined]

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