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Randomized Clinical Trial on peri-operative interventions for fragile older patients undergoing surgery. The Profyd trial.

Randomized Clinical Trial on peri-operative interventions for fragile older patients undergoing surgery. The Profyd trial. - Better in / Better out

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON38365
Enrollment
80
Registered
2011-06-29
Start date
2011-09-01
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

preventie van complicaties en functionele achteruitgang na electieve thorax- en buikchirurgie faster return to home optimal interdisciplinary collaboration

Interventions

The intervention group starts immediately with pre-surgical interventions adjusted to the patients* status. Daily activities and the patient*s fitness level are trained by a physiotherapist, the pat

Sponsors

Catharina-ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Elderly with an age above 70 years The elderly person lives independently or in an assisted living The erderly person undergoes an elective curative operation of abdomen/ thorax, during which the abdomen/ thorax is opened. They have to be vulnerable on at least 1 of the 4 criteria; delirium, number of falls, malnutrition and physical constraints. They have to live close to the hospital.;See document C1 Researchprotocol chapter 4.2 on page 14

Exclusion criteria

Exclusion criteria: Severe dementia (Clinical Dementia Rating >=2) Unsufficient understanding of the Dutch language to be able to understand instructions. This holds true for the patient him-/herself but also for the caregiver.;See document C1 Researchprotocol chapter 4.3

Design outcomes

Primary

MeasureTime frame
The primary outcome measures are complications after surgery and the length of stay in the hospital.

Secondary

MeasureTime frame
The secondary outcome measures are participation, quality of life, activities of daily life and the nutritional status.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)