Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01368120 · ClinicalTrials.gov registry record · Phase 1
Antimicrobial Activity of IV Clear™ Dressing - Prevention of Antimicrobial Regrowth
A Phase 1 study, sponsored by Covalon Technologies.
- Completed
- Registry status
- Phase 1
- Development phase
- 37
- Enrollment target
NCT01368120: Completed Phase 1 study, sponsored by Covalon Technologies.
NCT01368120 is a Phase 1 study that has completed, run by Covalon Technologies. The registered enrollment target is 37 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01368120, a Phase 1 study, has completed, sponsored by Covalon Technologies.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 37 participants
- Enrollment target
Study Summary
The purpose of this study is to assess the surface cutaneous antimicrobial activity of IV Clear™ Dressing, Tegaderm CHG™ Dressing and a Silicone Vehicle Control Dressing.
Primary Outcome
Mean number of Colony Forming Units (CFUs) per square centimetre (cm²) of skin prior to treatment (baseline), following prepping with 70% isopropyl alcohol and following post treatment samplings of IV Clear™, Tegaderm™ CHG and Silicone control dressings collected.
Interventions
- DEVICE Tegaderm CHG™
- DEVICE Silicone Vehicle Control Dressing
- DEVICE IV Clear™ Dressing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2011-04 |
| Est. Completion | 2011-07 |
| Phase | Phase 1 |
What the finished NCT01368120 record still lists
NCT01368120 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% lower).
The record links to 0 conditions, and to 3 interventions - of which Tegaderm CHG™ is the first listed.
NCT01368120 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01368120 about?
NCT01368120 is a clinical study titled "Antimicrobial Activity of IV Clear™ Dressing - Prevention of Antimicrobial Regrowth". The purpose of this study is to assess the surface cutaneous antimicrobial activity of IV Clear™ Dressing, Tegaderm CHG™ Dressing and a Silicone Vehicle Control Dressing.
What is the current status of trial NCT01368120?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 37 participants. The study started on 2011-04. Estimated completion is 2011-07.
What interventions are being tested in trial NCT01368120?
The interventions under investigation include: Tegaderm CHG™ (DEVICE), Silicone Vehicle Control Dressing (DEVICE), IV Clear™ Dressing (DEVICE).
Who is sponsoring clinical trial NCT01368120?
This trial is sponsored by Covalon Technologies, which has 4 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01368120's enrollment target sits among peer trials
37 1204th of 2000 higher than 791 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT02800486 · 37 participants · Phase 2
Super Selective Intra-arterial Repeated Infusion of Cetuximab (Erbitux) With Reirradiation for Treatment of Relapsed/Refractory GBM, AA, and AOA
- NCT03173937 · 37 participants · Phase 1
Unrelated Umbilical Cord Blood Transplantation for Severe Aplastic Anemia and Hypo-plastic MDS Using CordIn(TM), Umbilical Cord Blood-Derived Ex Vivo Expanded Stem and Progenitor Cells to Expedite Engraftment and Improve Transplant Outcome
- NCT03295227 · 37 participants · Phase 1
Pembrolizumab in Treating Participants With Unresectable Thymoma or Thymic Cancer
- NCT03401047 · 37 participants · Early Phase 1
Study to Assess Potential Impairments in Estradiol Augmentation of Gonadotropin Secretion in Polycystic Ovary Syndrome
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia