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The Effect of Darbepoetin Upon Rehabilitation for Colorectal Cancer Surgery

The Effect of Darbepoetin Alfa Treatment Upon the Rehabilitation Following Planned Surgery for Colorectal Cancer

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00122720
Enrollment
200
Registered
2005-07-22
Start date
2003-06-30
Completion date
2006-01-31
Last updated
2006-07-07

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

Conditions

Colorectal Cancer

Keywords

colorectal cancer, erythropoietin, rehabilitation, physical capacity

Brief summary

The study is investigating whether randomization to perioperative darbepoetin alfa treatment improves the rehabilitation following surgery for colonic and rectal cancer.

Detailed description

Major surgery elicits a metabolic stress response that is followed by a loss of body mass, fatigue, and an impaired physical performance including a reduced work capacity. To perform ordinary daily activities many elderly people exert close to their maximum physical capacity, and even a small reduction of performance capacity may cause significant impairment in physical and social activity. Postoperative decline in strength and work capacity may thus cause previously independent living persons to become dependent upon assistance from others. Hence, it is important to avoid the postoperative reduction of physical performance and to minimize postoperative fatigue. It has been shown that Erythropoietin treatment reduces the need for blood transfusions in patients undergoing planned colonic surgery. However, the effect of Erythropoietin treatment upon postoperative rehabilitation has not yet been studied. Therefore the main hypothesis in this study is that perioperative treatment with Darbepoetin Alfa would improve the physical capacity in aspects by reducing postoperative fatigue and improve work capacity, balance and quality of life compared to placebo treatment. Furthermore, the researchers expect Darbepoetin treated patients to have fewer perioperative complications and less need for blood transfusions.

Interventions

DRUGDarbepoetin Alfa

Sponsors

Amgen
CollaboratorINDUSTRY
Herning Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Planned colonic and rectal surgery because of presumed cancer disease in the colon and rectum

Exclusion criteria

* Psychiatric disease or dementia * Diseases, that renders participation in the study impossible * Thromboembolic disease within the last three months * Dysregulated hypertension (systolic blood pressure\>175 mmHg and/or diastolic blood pressure\>105 mmHg) * Other diseases or causes that will contraindicate treatment with Darbepoetin Alfa * Other diseases or causes that will contraindicate further treatment with Darbepoetin Alfa * Patients that preoperatively and/or four days postoperatively have a hemoglobin concentration \> 14 g/dl * Former cancer disease * Disseminated cancer disease * Rectal cancer stage T4

Design outcomes

Primary

MeasureTime frame
The functional capacity measured by postoperative fatigue, work capacity, balance, and quality of life

Secondary

MeasureTime frame
Muscular strength
Weight
Body composition
Blood transfusion
Postoperative complications

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026