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Effectiveness of CBD for Neuropathic Pain in Diabetic Foot Neuropathy

U

Universidad Complutense de Madrid

Status

Completed

Conditions

Neuropathic Pain Associated With Diabetic Peripheral Neuropathy
Xerosis Cutis

Treatments

Drug: Group 2. Cannabidiol and Urea 10% formula.
Drug: Group 3. Placebo formula.
Drug: Group 1. Complete formula

Study type

Interventional

Funder types

Other

Identifiers

NCT07162454
24/193-EC_X

Details and patient eligibility

About

Evaluation of cannabidiol and urea 10%.

Full description

This study evaluated the impact of cannabidiol on neuropathic pain and the action of urea 10% on skin quality in patients with diabetic foot syndrome and diabetic neuropathy.

Enrollment

23 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients all biological sexes
  • Patients of legal age (18 years).
  • Patients without cognitive impairment
  • Patients Diagnosed with diabetic neuropathy,
  • Patients who were able to complete the neuropathic pain scale autonomously, cooperatively and independently.

Exclusion criteria

  • Patients who declined participation
  • Patients with critical ischaemia and
  • Patients with a history of allergy or hypersensitivity to any of the components of the cream were excluded from the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

23 participants in 3 patient groups, including a placebo group

Group 1. Complete formula.
Experimental group
Description:
Participants in this group received a cream with cannabidiol, urea 10%, arnica and menthol as active ingredients during 1 month.
Treatment:
Drug: Group 1. Complete formula
Group 2. Cannabidiol and Urea 10% formula.
Experimental group
Description:
Participants in this group received a cream with cannabidiol, urea 10% as active ingredients during 1 month.
Treatment:
Drug: Group 2. Cannabidiol and Urea 10% formula.
Group 3. Base formula.
Placebo Comparator group
Description:
Participants in this group received a base cream with no active ingredients.
Treatment:
Drug: Group 3. Placebo formula.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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