Study of PEMF (Pulsed Electromagnetic Field) Therapy in the Treatment of

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Lumbar Surgery

See also
Status	Clinical Trial	Phase
Active, not recruiting	`NCT04562610` - Enhanced Recovery After Surgery in Orthopaedic Spine Surgery	Phase 2/Phase 3
Terminated	`NCT03118271` - Comparison of the Effect of Lumbar Traction, Spinal Manipulation, and Surgery in the Treatment of Lumbar Disc Herniation	N/A
Completed	`NCT01015651` - Assessment of the Nociception During Lumbar Surgery	N/A

See also

Status

Clinical Trial

Phase

Active, not recruiting

NCT04562610 - Enhanced Recovery After Surgery in Orthopaedic Spine Surgery

Phase 2/Phase 3

Terminated

NCT03118271 - Comparison of the Effect of Lumbar Traction, Spinal Manipulation, and Surgery in the Treatment of Lumbar Disc Herniation

N/A

Completed

NCT01015651 - Assessment of the Nociception During Lumbar Surgery

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	NCT02416973
Study type	Interventional
Source	Regenesis Biomedical, Inc.
Contact
Status	Active, not recruiting
Phase	N/A
Start date	March 2015

Study of PEMF (Pulsed Electromagnetic Field) Therapy in the Treatment of Persistent Post-Operative Pain Following Lumbar Surgery

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms