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Pilot Study to Characterize the Microbiome in Cutaneous T Cell Lymphoma Skin Lesions Before and After Use of CLn® Skin Care Body Wash

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Northwestern University

Status

Not yet enrolling

Conditions

Cutaneous T Cell Lymphoma

Treatments

Other: CLn Body Wash

Study type

Observational

Funder types

Other

Identifiers

NCT06665490
STU00222221

Details and patient eligibility

About

In this pilot study of patients with mycosis fungoides, the most common form of CTCL, we propose to primarily evaluate the impact of daily use of the CLn Body Wash (dilute sodium hypochlorite (0.006% NaOCl)) on the microbiota of CTCL lesions. Should dilute sodium hypochlorite body wash improve the microbiome of MF, reducing the abundance of S. aureus, future, larger studies can more fully evaluate the impact on pruritus, erythema, scaling, disease evolution and its role in CTCL management.

Enrollment

15 estimated patients

Sex

All

Ages

18 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults ages 18-89 years of age with active mycosis fungoides.
  • Patients with concurrent and prior malignancies are allowed as long as any concurrent malignancy does not directly involve the same skin site.

Exclusion criteria

  • Patients currently or recently (within past 4 weeks) on topical or systemic antibiotics, pregnant persons, or persons with potential of becoming pregnant or are/will be breastfeeding
  • Patients that have initiated a new skin-directed therapy over the past month.

Trial design

15 participants in 1 patient group

Mycosis Fungoides patients
Description:
Patients with mycosis fungoides will be enrolled at Northwestern Memorial Hospital Dermatology
Treatment:
Other: CLn Body Wash

Trial contacts and locations

1

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Central trial contact

Dermatology CTU

Data sourced from clinicaltrials.gov

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