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CBD cream shows promise for chemo nerve pain in small trial

NCT ID NCT05388058

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a topical cannabidiol (CBD) cream against a placebo cream to see if it could reduce nerve pain, numbness, and tingling in the hands and feet caused by chemotherapy. Forty adults with moderate to severe chemotherapy-induced peripheral neuropathy (CIPN) applied the cream daily for four weeks. The goal was to find a well-tolerated option for a condition that is often hard to treat with standard medications.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

40 people

The number who actually took part.

Started

Jun 2022

Finished

Jul 2023

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age \>= 18 years * English speaking * Cancer diagnosis of any tumor type with chemotherapy-induced neuropathy * At least 4 out of 10 severity of neuropathy pain and/or tingling * Stable for at least 7 days prior to registration on medications for neuropathy, if any are being used * Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2 * Negative pregnancy test done =\< 7 days prior to registration, for persons of childbearing potential only * NOTE: If a urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required * Able to provide written informed consent * Ability to complete questionnaire(s) by themselves or with assistance * No evidence of residual cancer * Platelet count \> 100,000/mm\^3 (following completion of chemotherapy) * Absolute neutrophil count (ANC) \>= 1,000/mm\^3 (following completion of chemotherapy) * Hemoglobin \> 11 g/dL (following completion of chemotherapy) * Serum transaminase (alanine aminotransferase \[ALT\] or aspartate aminotransferase \[AST\]) =\< 1.2 x upper limit of normal (ULN) (following completion of chemotherapy) * Alkaline phosphatase =\< 1.2 x ULN (following completion of chemotherapy) * Serum creatinine =\< 1.2 x ULN (following completion of chemotherapy) Exclusion Criteria: * Any of the following because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown: * Pregnant persons * Nursing persons * Persons of childbearing potential who are unwilling to employ adequate contraception * Any medical condition that would prohibit use of a topical cream (skin infection or open wound in the area of the neuropathy) * Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens * Pre-existing neuropathy prior to chemotherapy that would confuse the issue of CIPN * Currently on chemotherapy or received chemotherapy treatment within the prior 3 months * Use of other cannabis products within 30 days prior to registration * History of allergy to cannabis products

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Fairview Grand Itasca Clinic and Hospital

    Grand Rapids, Minnesota, 55744, United States

  • Fairview Northland Medical Center

    Princeton, Minnesota, 55371, United States

  • Fairview Range Medical Center

    Hibbing, Minnesota, 55746, United States

  • Mayo Clinic Health System Albert Lea

    Albert Lea, Minnesota, 56007, United States

  • Mayo Clinic Health System Mankato

    Mankato, Minnesota, 56001, United States

  • Mayo Clinic in Rochester

    Rochester, Minnesota, 55905, United States

  • Monticello Cancer Center

    Monticello, Minnesota, 55362, United States

  • Sanford Thief River Falls

    Thief River Falls, Minnesota, 56701, United States

  • Sanford Worthington

    Worthington, Minnesota, 56187, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.