Rapid Rehabilitation to Treat Lower Extremity Trauma

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT06195540` - RIVAroxaban Versus Low-molecular Weight Heparin in Patients With Lower Limb Trauma Requiring Brace or CASTing	Phase 3
Recruiting	`NCT06416280` - Inter-observer Reliability of the TRiP(Cast) Score in Patients With Trauma to a Lower Limb Requiring Immobilisation
Completed	`NCT04064489` - Thromboembolic Risk Stratification by TRiP(Cast) Score to Guide Physicians in Preventive Treatment Prescriptions for Patients With Lower Limb Trauma Requiring Brace or castING.	N/A

See also

Status

Clinical Trial

Phase

Not yet recruiting

NCT06195540 - RIVAroxaban Versus Low-molecular Weight Heparin in Patients With Lower Limb Trauma Requiring Brace or CASTing

Phase 3

Recruiting

NCT06416280 - Inter-observer Reliability of the TRiP(Cast) Score in Patients With Trauma to a Lower Limb Requiring Immobilisation

Completed

NCT04064489 - Thromboembolic Risk Stratification by TRiP(Cast) Score to Guide Physicians in Preventive Treatment Prescriptions for Patients With Lower Limb Trauma Requiring Brace or castING.

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	NCT05225792
Study type	Interventional
Source	Mayo Clinic
Contact	Christine Huyber, CCRP
Phone	(507) 266-0984
Email	Huyber.Christine@mayo.edu
Status	Recruiting
Phase	N/A
Start date	January 8, 2024
Completion date	April 2026

Rapid Rehabilitation to Treat Lower Extremity Trauma

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms