Psychophysical Studies of Cancer Therapy Pain
Launched by M.D. ANDERSON CANCER CENTER · Aug 10, 2007
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
**Trial Summary: Psychophysical Studies of Cancer Therapy Pain**
This clinical trial is looking into how cancer treatments can cause pain and how we can better understand it. Researchers want to see if special tests can help us learn more about the nerve pain that some patients experience after receiving cancer therapies like chemotherapy. By taking small skin samples from patients who have pain from these treatments, the study aims to find out if the nerve damage is due to a loss of nerve connections in the skin.
To participate in this trial, individuals must be at least 18 years old and either currently experiencing pain from cancer treatments or about to start chemotherapy without having pain yet. Participants will undergo some tests that might cause mild discomfort, but these are designed to help researchers gather important information. This study is open to all genders, and it is currently recruiting participants. If you're interested or think you might qualify, it’s a good idea to discuss it with your healthcare provider.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Since moderate pain, albeit brief, will be induced, this feasibility project will be limited to consenting adults, 18 years old or older, in which there is also a well established QST database.
- • 2. The subjects must be able to understand the nature of the study and have signed consent.
- • 3. The patients must either: a) have pain that has developed as a consequence of cancer therapy with either vinca alkaloids, taxanes, bortezomib, thalidomide, platinum-based compounds or ionizing irradiation. OR b) have no pain that has developed as a consequence of cancer therapy, and are just entering chemotherapy with taxanes, vinka alkaloids, bortezomib, thalidomide, or platinum-based compounds
- • 4. (For Healthy Controls) Willing to participate and have signed an informed consent.
- Exclusion Criteria:
- • 1. Patients who refuse to participate or who are determined incapable of completing the research.
- • 2. (For Healthy Controls) Receiving anti-coagulants, immunosuppressed or diabetic.
About M.D. Anderson Cancer Center
The University of Texas MD Anderson Cancer Center is a leading institution dedicated to cancer care, research, education, and prevention. As one of the world’s most respected cancer centers, MD Anderson focuses on innovative treatment approaches and groundbreaking clinical trials aimed at improving patient outcomes. With a multidisciplinary team of experts and state-of-the-art facilities, the center is committed to advancing cancer research and providing comprehensive, personalized care to patients. MD Anderson's clinical trials play a pivotal role in translating scientific discoveries into effective therapies, positioning the center at the forefront of cancer treatment and research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Houston, Texas, United States
Patients applied
Trial Officials
Patrick M. Dougherty, PhD
Principal Investigator
M.D. Anderson Cancer Center
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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