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The Effect of Darbepoetin Upon Rehabilitation for Colorectal Cancer Surgery

Primary Purpose

Colorectal Cancer

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Darbepoetin Alfa
Sponsored by
Herning Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Cancer focused on measuring colorectal cancer, erythropoietin, rehabilitation, physical capacity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Surgical Department, Middelfart Hospital
  • Surgical Department, Odense University Hospital
  • Surgical Department, Svendborg Hospital
  • Surgical Department, Herning Hospital
  • Surgical Department, Aarhus University Hospital

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Muscular strength
Weight
Body composition
Blood transfusion
Postoperative complications

Full Information

First Posted
July 20, 2005
Last Updated
July 3, 2006
Sponsor
Herning Hospital
Collaborators
Amgen
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1. Study Identification

Unique Protocol Identification Number
NCT00122720
Brief Title
The Effect of Darbepoetin Upon Rehabilitation for Colorectal Cancer Surgery
Official Title
The Effect of Darbepoetin Alfa Treatment Upon the Rehabilitation Following Planned Surgery for Colorectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
January 2006
Overall Recruitment Status
Completed
Study Start Date
June 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Herning Hospital
Collaborators
Amgen

4. Oversight

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
colorectal cancer, erythropoietin, rehabilitation, physical capacity

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
Double
Allocation
Randomized
Enrollment
200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Darbepoetin Alfa
Primary Outcome Measure Information:
Title
The functional capacity measured by postoperative fatigue, work capacity, balance, and quality of life
Secondary Outcome Measure Information:
Title
Muscular strength
Title
Weight
Title
Body composition
Title
Blood transfusion
Title
Postoperative complications

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charlotte B Norager, M.D.
Organizational Affiliation
Surgical Research Department, Herning Hospital, Gl. Landevej 61, DK-7400 Herning
Official's Role
Principal Investigator
Facility Information:
Facility Name
Surgical Department, Middelfart Hospital
City
Middelfart
State/Province
Fyn
ZIP/Postal Code
5500
Country
Denmark
Facility Name
Surgical Department, Odense University Hospital
City
Odense
State/Province
Fyn
ZIP/Postal Code
5000
Country
Denmark
Facility Name
Surgical Department, Svendborg Hospital
City
Svendborg
State/Province
Fyn
ZIP/Postal Code
5700
Country
Denmark
Facility Name
Surgical Department, Herning Hospital
City
Herning
State/Province
Ringkobing
ZIP/Postal Code
7400
Country
Denmark
Facility Name
Surgical Department, Aarhus University Hospital
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark

12. IPD Sharing Statement

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The Effect of Darbepoetin Upon Rehabilitation for Colorectal Cancer Surgery

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