A Multi-center, Randomized, Subject Blind, Active Controlled Design

See also
Status	Clinical Trial	Phase
Completed	`NCT03512717` - Efficacy and Safety of Potenfill for Temporary Penile Enhancement	N/A
Completed	`NCT03153735` - Clinical Study to CMDHA0101 as Compared to PowerFill® for Temporary Penile Enhancement	N/A
Completed	`NCT03840070` - The Efficacy and Safety of Repeat-dose Potenfill for Temporary Penile Enhancement	N/A
Completed	`NCT04496427` - Observational Study to Determine the Efficacy and Safety of Potenfill for Temporary Penile Enhancement

See also

Status

Clinical Trial

Phase

Completed

NCT03512717 - Efficacy and Safety of Potenfill for Temporary Penile Enhancement

N/A

Completed

NCT03153735 - Clinical Study to CMDHA0101 as Compared to PowerFill® for Temporary Penile Enhancement

N/A

Completed

NCT03840070 - The Efficacy and Safety of Repeat-dose Potenfill for Temporary Penile Enhancement

N/A

Completed

NCT04496427 - Observational Study to Determine the Efficacy and Safety of Potenfill for Temporary Penile Enhancement

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT02833532
Study type	Interventional
Source	Hugel
Contact
Status	Completed
Phase	Phase 3
Start date	June 2015
Completion date	June 2017

A Multi-center, Randomized, Subject Blind, Active Controlled Design Clinical Study to Evaluate the Efficacy and Safety of Volus as Compared to PowerFill® for Temporary Penile Enhancement

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms