This study will be performed to test the predictive value of the GFI, the VES-13 and the timed “up and go” test compared to components of PACE in elderly patients of the age of 70 years and above undergoing surgery for a solid tumour.
ID
Bron
Verkorte titel
Aandoening
Surgical oncology
Elderly
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
- Primary endpoint will be 30 day morbidity and mortality.
Achtergrond van het onderzoek
-
Doel van het onderzoek
This study will be performed to test the predictive value of the GFI, the VES-13 and the timed “up and go” test compared to components of PACE in elderly patients of the age of 70 years and above undergoing surgery for a solid tumour.
Onderzoeksopzet
Data will be collected preoperatively and up to 30 days postoperatively
Onderzoeksproduct en/of interventie
The combination of components of PACE, the timed “up and go” test, the VES-13 and the GFI will be administered to every patient within two weeks prior to the surgical procedure. This can be done by a nurse in the preoperative clinic and will take approximately 30 minutes.
Patient data will be recorded during the length of the hospital stay, the patient file will be used to retrieve these data.
Preoperative data:
- medication used
- living situation
- comorbidity
- nutritional status.
Perioperative data:
- type of surgery
- duration of anaesthesia
- blood loss
- length of hospital stay
- postoperative complications
- consultation by other specialist.
Follow up: at the postoperative visit to the outpatient clinic additional data on morbidity occurring during the first 30 days postoperatively can be recorded as well as any additional specialists that were involved in patient care in the first 30 postoperative days.
Publiek
P.O. Box 30.001
B.L. Leeuwen, van
Groningen 9700 RB
The Netherlands
+31 (0)50 3612301
blvleeuwen@hetnet
Wetenschappelijk
P.O. Box 30.001
B.L. Leeuwen, van
Groningen 9700 RB
The Netherlands
+31 (0)50 3612301
blvleeuwen@hetnet
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Patients aged >70 years undergoing elective surgery for a solid tumour under general anaesthesia will be included for this study.
- Patients will be stratified according to tumour localisation: intra cavity (e.g. colorectal, gynaecological) vs superficial (e.g. breast, head & neck, melanoma).
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Patients not able to give informed consent
Opzet
Deelname
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL1497 |
| NTR-old | NTR1567 |
| Ander register | : |
| ISRCTN | ISRCTN wordt niet meer aangevraagd |