Other Clinical Trial - MFR Versus PFS Techniques on Pain,Range of Motion

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT06116058` - Integrated Neuromuscular Inhibition Versus Instrument Assisted Soft Tissue Mobilization in Chronic Back Pain	N/A
Not yet recruiting	`NCT05232435` - Pilate Mat Exercise Versus Muscle Energy Technique on Chronic Non Specific Low Back Pain	N/A
Completed	`NCT03016676` - Efficacy of SM on Postural Instability and Quality of Life in Patients With Chronic Non Specific Low Back Pain(CNSLBP)	N/A

See also

Status

Clinical Trial

Phase

Not yet recruiting

NCT06116058 - Integrated Neuromuscular Inhibition Versus Instrument Assisted Soft Tissue Mobilization in Chronic Back Pain

N/A

Not yet recruiting

NCT05232435 - Pilate Mat Exercise Versus Muscle Energy Technique on Chronic Non Specific Low Back Pain

N/A

Completed

NCT03016676 - Efficacy of SM on Postural Instability and Quality of Life in Patients With Chronic Non Specific Low Back Pain(CNSLBP)

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	NCT05811260
Study type	Interventional
Source	Riphah International University
Contact
Status	Completed
Phase	N/A
Start date	March 31, 2023
Completion date	August 1, 2023

MFR Versus PFS Techniques on Pain,Range of Motion And Disability in Chronic Non Specific Low Back Pain.

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms