Mayo Clinic Health Connection Discovery Trial

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research

Related Conditions & MeSH terms

Surgical Recovery

See also
Status	Clinical Trial	Phase
Active, not recruiting	`NCT04732000` - Oxidative Stress and Surgical Recovery	Phase 2
Not yet recruiting	`NCT04266106` - Probiotics and Recovery From Gastrointestinal Surgery - 2	Phase 3
Completed	`NCT03123068` - Cocoa Flavanols for Modulating Immune Response and Accelerating Recovery	Phase 1/Phase 2

See also

Status

Clinical Trial

Phase

Active, not recruiting

NCT04732000 - Oxidative Stress and Surgical Recovery

Phase 2

Not yet recruiting

NCT04266106 - Probiotics and Recovery From Gastrointestinal Surgery - 2

Phase 3

Completed

NCT03123068 - Cocoa Flavanols for Modulating Immune Response and Accelerating Recovery

Phase 1/Phase 2

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	NCT01777841
Study type	Interventional
Source	Mayo Clinic
Contact
Status	Completed
Phase	N/A
Start date	February 2012
Completion date	January 2013

Mayo Clinic Health Connection Discovery Trial

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms