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Acupuncture in Treating Mucositis-Related Pain Caused by Chemotherapy in Patients Undergoing Stem Cell Transplantation



Acupuncture in Treating Mucositis-Related Pain Caused by Chemotherapy in Patients Undergoing Stem Cell Transplantation

For Condition: Cancer,oral complications of cancer and cancer therapy,Pain
Status: Recruiting
Sponsor(s): National Cancer Institute (NCI) ,
Synopsis: RATIONALE: Acupuncture may be effective in relieving mucositis-related pain caused by chemotherapy in patients undergoing stem cell transplantation. PURPOSE: Randomized clinical trial to study the effectiveness of acupuncture in treating mucositis-related pain caused by high-dose chemotherapy in patients who are undergoing stem cell transplantation.
Details: OBJECTIVES: - Compare the efficacy of acupuncture vs placebo acupuncture in alleviating mucositis-related pain secondary to high-dose chemotherapy, as assessed by total cumulative dose of opioids used and subjective pain scores, in patients undergoing hematopoietic stem cell transplantation. - Compare the overall number of patients requiring opioid therapy in these 2 intervention groups. - Compare the nausea and vomiting scores of patients in these 2 intervention groups. - Compare the sedation score of patients in these 2 intervention groups. - Compare the use of other psychotropic medications (e.g., anxiolytics or hypnotics) in patients in these 2 intervention groups. - Compare the need for total parenteral nutrition (TPN) and the number of days on TPN experienced by patients in these 2 intervention groups. - Compare pruritus and the need for symptomatic treatment in patients in these 2 intervention groups. OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are stratified according to 9-phenylthiocarbamide/6-n-propylthiouracil (PROP) tasting ability (super-tasters vs non-super-tasters). Patients are randomized to 1 of 2 treatment arms. - Arm I: Beginning immediately after the development of mucositis pain, patients undergo acupuncture over 30 minutes once daily. Patients also receive standard pain management. Treatment continues until pain is completely resolved in the absence of unacceptable toxicity. - Arm II: Patients undergo placebo acupuncture and receive standard pain management as in arm I. PROJECTED ACCRUAL: A maximum of 45 patients will be accrued for this study within 3 years.
Eligibility:
Study Type:  Interventional, Treatment
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: DISEASE CHARACTERISTICS: - Must be undergoing hematopoietic stem cell transplantation (HSCT) through one of the following means: - Concurrent enrollment on a HSCT protocol with the Experimental Transplantation & Immunology Branch (ETIB) at the NCI Center for Clinical Research* - Receiving HSCT as a compassionate exemption following the clinical guidelines of an ETIB protocol* - Directly observed oral or pharyngeal mucositis and/or suspected esophageal mucositis after high-dose chemotherapy - No pain unrelated to mucositis requiring use of potent analgesics prior to initiation of high-dose chemotherapy NOTE: *Protocol must be known to generate more than 50% incidence of high-dose chemotherapy-induced mucositis PATIENT CHARACTERISTICS: Age - 18 and over Performance status - Not specified Life expectancy - Not specified Hematopoietic - No history of bleeding disorders Hepatic - PT and PTT normal Renal - Not specified Other - No history or evidence of drug addiction or drug-seeking behavior - No skin infection at the sites of acupuncture points PRIOR CONCURRENT THERAPY: Biologic therapy - See Disease Characteristics Chemotherapy - See Disease Characteristics Endocrine therapy - Not specified Radiotherapy - Not specified Surgery - Not specified Other - No concurrent anticoagulant therapy
Total Enrollment: 

Location and Contact Information:

Overall Study Official:
ClaudeKasten-Sportes,  Study Chair,  National Cancer Institute (NCI)

Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support *Recruiting*
Bethesda,  Maryland,  20892-1182
United States
Recruiting Patient  Recruitment 888-NCI-1937


Additional Information:
Study ID Numbers:  CDR0000299048;  NCI-03-C-0125
Study Start Date: 
Record last reviewed: April 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00060021

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