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Clinical Trials/NL-OMON44014
NL-OMON44014
Completed
Not Applicable

A randomized, double-blind, placebo-controlled study to investigate the effects of an 8-week recombinant human erythropoietin (NeoRecormon) treatment on well-trained cyclists and their cycling performance. - Erythropoetine effects on cycling performance.

Centre for Human Drug Research0 sites48 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fietsprestatie
Sponsor
Centre for Human Drug Research
Enrollment
48
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Trial is onging in other countries

Registry
who.int
Start Date
TBD
End Date
August 15, 2016
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Well\-trained (as determined by cycling history and maximal power output \>4 W/kg) male subjects, 18 to 50 years old (inclusive);
  • 2\. Subjects must be healthy / medically stable on the basis of clinical laboratory tests, medical history, vital signs, and 12\-lead ECG performed at screening, including exercise ECG.
  • 3\. Each subject must sign an informed consent form prior to the study. This means the subject understands the purpose of and procedures required for the study.

Exclusion Criteria

  • 1\. Any clinically significant abnormality, as determined by medical history taking and physical examinations, obtained during the screening visit that in the opinion of the investigator would interfere with the study objectives or compromise subject safety.
  • 2\. Unacceptable known concomitant diagnoses or diseases at baseline, e.g., known cardiovascular, pulmonary, muscle, metabolic or haematological disease, renal or liver dysfunction, ECG or laboratory abnormalities, etc.
  • 3\. Unacceptable concomitant medications at baseline, e.g., drugs known or likely to interact with the study drugs or study assessments.
  • 4\. Unacceptable potential cycling performance enhancing medications at baseline, e.g. Erythropoiesis\-stimulating agents, Anabolic Androgenic Steroids, Growth Hormone, Insulin, IGF\-I and Beta\-Adrenergic Agents or methods, e.g. altitude tents.
  • 5\. Blood transfusion in the past three months.
  • 6\. Loss or donation of blood over 500 mL within three months.
  • 7\. Participation in a clinical trial within 90 days of screening or more than 4 times in the previous year.
  • 8\. Known hypersensitivity to the treatment or drugs of the same class, or any of their excipients.
  • 9\. Any known factor, condition, or disease that might interfere with treatment compliance, study conduct or interpretation of the results such as drug or alcohol dependence or psychiatric disease.
  • 10\. Positive urine drug test at screening

Outcomes

Primary Outcomes

Not specified

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