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NCT03153735
Clinical Study to CMDHA0101 as Compared to PowerFill® for Temporary Penile Enhancement
NA trial testing CMDHA0101 in Small Penis in 68 participants. Completed in 7 November 2017.
7 November 2017
Quick facts
| Lead sponsor | CHA MEDITECH Co., Ltd. |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 68 |
| Start date | 2 December 2016 |
| Primary completion | 7 November 2017 |
| Estimated completion | 7 November 2017 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- CMDHA0101
- PowerFill®
Conditions studied
- Small Penis — all drugs for Small Penis →
- Penile Enhancement — all drugs for Penile Enhancement →
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):
-
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:
- PubMed search for NCT03153735
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03153735 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by CHA MEDITECH Co., Ltd.
- Last refreshed: 12 December 2017
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