Last reviewed · How we verify

NCT03153735

Clinical Study to CMDHA0101 as Compared to PowerFill® for Temporary Penile Enhancement

Completed NA Last updated 12 December 2017
What this trial tests

NA trial testing CMDHA0101 in Small Penis in 68 participants. Completed in 7 November 2017.

Timeline
2 December 2016
Primary endpoint
7 November 2017
7 November 2017

Quick facts

Lead sponsorCHA MEDITECH Co., Ltd.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment68
Start date2 December 2016
Primary completion7 November 2017
Estimated completion7 November 2017
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

CHA MEDITECH Co., Ltd.

Who can join

Adults 20 to 65, male only, with Small Penis or Penile Enhancement. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The investigators aimed to confirm the efficacy and safety of transdermal penis enlargement for 24 weeks after CMDHA0101 injection in subjects who wanted penile enlargement in male patients with small-penis syndrome \*. \*Small-penis syndrome is the anxiety of thinking one's penis is too small - even though it isn't.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Comparison of Clinical Outcomes between Hyaluronic and Polylactic Acid Filler Injections for Penile Augmentation in Men Reporting a Small Penis: A Multicenter, Patient-Blinded/Evaluator-Blinded, Non-Inferiority, Randomized Comparative Trial with 18 Months of Follow-up.
    Yang DY, Jeong HC, Ko K, Lee SH, et al · · 2020 · cited 19× · PMID 32260508 · DOI 10.3390/jcm9041024

Verify or expand the search:

Verify against primary sources

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/NCT03153735.

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