Effects of Topical Cream for Pain Relief

Natural Immune Systems

Status

Completed

Conditions

Chronic Pain

Treatments

Other: Topical cream

Study type

Interventional

Funder types

Other

Identifiers

NCT05213052

173-001

Details and patient eligibility

About

To perform a clinical proof-of-concept study on a novel topical formula for pain relief.

Full description

An open-label study where each participant will be involved in the study for 4 weeks. During the study participants will use the topical cream 1-2 times daily on the anatomical area(s) causing the most pain.

Enrollment

12 patients

Sex

All

Ages

21 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

BMI between 18.5 and 34.9 kg/m2 (inclusive)
Chronic joint/muscle related pain for at least past 6 months
Experiencing chronic pain in at least one specific anatomical area for more than 6 months.

Exclusion criteria

Cancer during past 12 months
Chemotherapy during past 12 months
Currently taking prescription pain medications
Getting regular joint injections (such as cortisone shots);
Immunization during last month
Participation in another clinical trial study during this trial, involving an investigational product or lifestyle change
Regularly experiencing headaches, including migraines
Serious active illness within past 6 months
Significant active uncontrolled illness (such as lymphoma, liver disease, kidney failure, heart failure).
Skin allergies related to ingredients in test product.