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NCT03114514

Efficacy of Platelet-rich Plasma (PRP) in the Treatment of Dark Circles Under the Eyes

Completed NA Last updated 16 May 2017
What this trial tests

NA trial testing PRP in Periorbital Hyperpigmentation in 40 participants. Completed in 10 May 2017.

Timeline
17 June 2016
Primary endpoint
20 April 2017
10 May 2017

Quick facts

Lead sponsorDamascus University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment40
Start date17 June 2016
Primary completion20 April 2017
Estimated completion10 May 2017
Sites1 location across Syria

Drugs / interventions tested

Conditions studied

Sponsor

Damascus University

Who can join

Adults 15 to 65, any sex, with Periorbital Hyperpigmentation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

10 ml of blood from each patient will be drawn. This blood specimen will be centrifuged in a specific way to get 1 ml of platelet rich plasma (PRP). PRP will be injected into the the skin under the eyes. The treatment course consists of three sessions of PRP injections with one-month intervals between the sessions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of PRP

Trials testing the same drug.

Other Damascus University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03114514.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing