LiquiBand Versus Dermabond Versus Sutures for Closure of Surgical Wounds

See also
Status	Clinical Trial	Phase
Completed	`NCT03020420` - Clinical Trial To Study The Anti-scarring Effect Of Cicatricell	N/A
Withdrawn	`NCT00872638` - The Effect of Wound Edge Eversion on Cosmesis	N/A
Completed	`NCT00557947` - Prineo (Dermabond Protape) Versus Sutures for Full-thickness Surgical Incisions	Phase 4
Completed	`NCT00890578` - HISTOACRYL: A Study of Its Efficacy in Final Scar Formation	Phase 4

See also

Status

Clinical Trial

Phase

Completed

NCT03020420 - Clinical Trial To Study The Anti-scarring Effect Of Cicatricell

N/A

Withdrawn

NCT00872638 - The Effect of Wound Edge Eversion on Cosmesis

N/A

Completed

NCT00557947 - Prineo (Dermabond Protape) Versus Sutures for Full-thickness Surgical Incisions

Phase 4

Completed

NCT00890578 - HISTOACRYL: A Study of Its Efficacy in Final Scar Formation

Phase 4

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	NCT01835405
Study type	Interventional
Source	Advanced Medical Solutions (Plymouth) Ltd
Contact
Status	Completed
Phase	N/A
Start date	February 20, 2013
Completion date	February 14, 2014

LiquiBand Versus Dermabond Versus Sutures for Closure of Surgical Wounds

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms