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Use of Platelet-rich Plasma (PRP) Therapy in Patients With Brittle Nail Syndrome

Weill Cornell Medicine (WCM) logo

Weill Cornell Medicine (WCM)

Status and phase

Completed
Phase 4

Conditions

Nail Diseases

Treatments

Device: Platelet-poor plasma
Device: Platelet-rich plasma

Study type

Interventional

Funder types

Other

Identifiers

NCT04941807
20-07022437

Details and patient eligibility

About

The purpose of this study is to assess the efficacy and safety of platelet-rich plasma therapy for brittle nail syndrome

Enrollment

11 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who have been diagnosed with brittle nails
  • Must understand and voluntarily sign an informed consent form
  • Must be male or female and aged 18-95 years at time of consent
  • Must be able to adhere to the study visit schedule and other protocol requirements
  • A nail clipping with histopathology that is negative for the presence of dermatophyte infection
  • Patient must present with at least a score of 2 on the PGA scale.

Exclusion criteria

  • Inability of the patient to provide written informed consent for any reason.

    • Subject has psoriasis, lichen planus, dermatophyte infection or other confounding abnormalities that are severe enough to result in a clinically abnormal fingernail
    • Use of any medication within 90 days prior to start of study
    • Inability to abstain for nail polishes, nail gels during the study period
    • Subject is pregnant or planning pregnancy.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

11 participants in 2 patient groups, including a placebo group

Platelet-rich plasma
Experimental group
Description:
The proximal nail fold is cleansed with alcohol and platelet-rich plasma obtained from the patient is injected using a 1ml syringe and 30g needle, 0.1-0.2 ml of platelet-rich plasma is injected into 8 proximal nail folds.
Treatment:
Device: Platelet-rich plasma
Platelet-poor plasma
Placebo Comparator group
Description:
The proximal nail fold is cleansed with alcohol and platelet-poor plasma obtained from the patient is injected using a 1ml syringe and 30g needle, 0.1-0.2 ml of platelet-poor plasma is injected into 2 proximal nail folds.
Treatment:
Device: Platelet-poor plasma

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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