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Preoperative risk estimation for onco-geriatric patients.

A clinical trial for the comparison of different preoperative assessment tools in the elderly surgical patient.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON29384
Enrollment
362
Registered
2008-11-28
Start date
2008-09-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Surgical oncology Elderly

Interventions

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

Sponsors

No sponsors
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - 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).

Exclusion criteria

Exclusion criteria: - Patients not able to give informed consent

Design outcomes

Primary

MeasureTime frame
- Primary endpoint will be 30 day morbidity and mortality.

Secondary

MeasureTime frame
- Secondary endpoints will be length of hospital stay and the number of additional specialists involved in patient care in the 30 days after surgery.

Contacts

Public ContactB.L. Leeuwen, van

University Medical Center Groningen (UMCG), Department of Surgery, P.O. Box 30.001

blvleeuwen@hetnet+31 (0)50 3612301

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)