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NCT04459416Active, not recruitingPhase 3

Managing Pain and Symptom Burden Caused by Chemotherapy in People With Myeloma or Lymphoma

Opioid-Sparing Pain Treatment In Myeloma And Lymphoma Patients Undergoing High-Dose Chemotherapy (OPTIMAL-HiChemo): Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 9 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to find out whether acupuncture treatments can reduce the need for opioid medication when managing pain caused by chemotherapy. The study will compare the effects of adding acupuncture to usual pain management with those of usual pain management alone, in reducing opioid use by relieving pain. Researchers also want to find out more about the effects of acupuncture treatments on other symptoms caused by cancer treatments and quality of life.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
299 (actual)
First submitted
1 Jul 2020
Start date
30 Jun 2020
Primary completion date
2 Jul 2024
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT04459416

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 299
  • From 30 Jun 2020 to the primary completion date, 2 Jul 2024
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • acupuncture within two weeks prior to HiChemo (to avoid residual effects of acupuncture)

Lab values

  • absolute neutrophil count (ANC) of \<500/μl, platelet count of \<20,000/ μl or INR \>2.0

Other

  • unable to provide informed consent

Who the study is looking for

  • age 18 or older
  • pathological diagnosis of MM, HD or NHL
  • scheduled for high dose chemotherapy for auto-HSCT in the following month (30 days)
  • not taking opioids regularly in the week prior to consent (one-time dosing of opioids for a painful procedure is allowed)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Seattle Cancel Care Alliance (Data Collection Only)
Coordinator of this site? Confirm its status
SeattleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.