Amputee Clinical Trial - The Effect of Silicone Suspension on Standing

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Amputee

See also
Status	Clinical Trial	Phase
Completed	`NCT04330274` - Comparison of Different Amputation Levels
Completed	`NCT00439088` - Try Walking a Mile in These Shoes: Activity Level of Lower Extremity Amputees	Phase 1
Completed	`NCT03825432` - Investigation of Physical Activity and Associated Factors in Lower Extremity Amputees

See also

Status

Clinical Trial

Phase

Completed

NCT04330274 - Comparison of Different Amputation Levels

Completed

NCT00439088 - Try Walking a Mile in These Shoes: Activity Level of Lower Extremity Amputees

Phase 1

Completed

NCT03825432 - Investigation of Physical Activity and Associated Factors in Lower Extremity Amputees

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	NCT00400127
Study type	Interventional
Source	Nova Scotia Health Authority
Contact
Status	Terminated
Phase	N/A
Start date	September 2005
Completion date	April 2007

The Effect of Silicone Suspension on Standing Balance for Transfemoral Amputees

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms