Last updated: March 17, 2021
Sponsor: Philips Healthcare
Overall Status: Completed
Phase
N/A
Condition
Cancer
Treatment
N/AClinical Study ID
NCT01436669
REC 10/H0724/14
Ages 19-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male or female, age > 18.
- Able to give informed written consent in the English language.
- Diagnosis of cancer and receiving chemotherapy or with a planned chemotherapy startdate within 2 weeks of enrolment.
- Patients who are able to perform finger prick test to obtain capillary blood.
Exclusion
Exclusion Criteria:
- Inability to give informed consent due to mental capacity or language problems.
- Patients at risk of bruising or bleeding as a result of their disease or treatment.
- Patients at risk of bruising or bleeding due to anticoagulants (heparin or warfarin),aspirin or thrombocytopenia (platelet count <80).
- Patients with diabetes mellitus
- Patients with peripheral neuropathy
Study Design
Total Participants: 20
Study Start date:
June 01, 2011
Estimated Completion Date:
May 31, 2012
Study Description
Connect with a study center
Royal Marsden Hospital
Belmont, Surrey
United KingdomSite Not Available
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.