Minimal Access Repair of Contralateral Hernias (MARCH Trial)

See also
Status	Clinical Trial	Phase
Recruiting	`NCT01830452` - Less Chronic Pain After Lichtenstein Hernioplasty Using the Self-gripping Parietex Progrip Mesh	Phase 4
Completed	`NCT02016443` - Tizanidine and Pain After Herniorrhaphy	Phase 4
Completed	`NCT01622712` - Evaluation of Mesh Integration and Mesh Contraction After Open Preperitoneal Inguinal Hernia Repair Using a Memory Ring Containing Device	N/A

See also

Status

Clinical Trial

Phase

Recruiting

NCT01830452 - Less Chronic Pain After Lichtenstein Hernioplasty Using the Self-gripping Parietex Progrip Mesh

Phase 4

Completed

NCT02016443 - Tizanidine and Pain After Herniorrhaphy

Phase 4

Completed

NCT01622712 - Evaluation of Mesh Integration and Mesh Contraction After Open Preperitoneal Inguinal Hernia Repair Using a Memory Ring Containing Device

N/A

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	NCT00293995
Study type	Interventional
Source	Institute of Child Health
Contact
Status	Completed
Phase	N/A
Start date	March 2006
Completion date	November 2013

Minimal Access Repair of Contralateral Hernias (MARCH Trial)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms