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Efficacy and Safety of Platelet-Rich Plasma As an Intraoperative Holding Solution in Hair Transplantation

B

Benha University

Status

Completed

Conditions

Hair Transplantation

Treatments

Other: Saline
Biological: Platelet rich plasma (PRP)

Study type

Interventional

Funder types

Other

Identifiers

NCT06849674
PRP in hair transplantation

Details and patient eligibility

About

The goal of this study is to determine the efficacy of using platelet-rich plasma (PRP) versus 0.9% normal saline as a storage solution during follicular unit extraction (FUE) hair transplantation.

Enrollment

60 patients

Sex

Male

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male patients who have androgenetic alopecia
  • Patients who are interested in having their hair transplanted

Exclusion criteria

  • Individuals with comorbidities
  • History of keloids or hypertrophic scarring
  • Low donor area density
  • Other causes of alopecia
  • Scalp infections
  • Patients with a bleeding tendency
  • Patients on anticoagulant therapy
  • Patients who are HIV-positive or Hepatitis B- or C-positive

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Saline group
Active Comparator group
Description:
in this group, hair grafts will be stored in Normal saline 0.9% before transplantation.
Treatment:
Other: Saline
Platelet-rich plasma group
Experimental group
Description:
In this group, hair grafts will be stored in Platelet-rich plasma before transplantation.
Treatment:
Biological: Platelet rich plasma (PRP)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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