Efficacy & Safety of Diclofenac Sodium Topical Gel 1% Applied Four Times

Clinical Trial Description

n/a

Study Design

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

See also
Status	Clinical Trial	Phase
Completed	`NCT01874626` - Efficacy and Safety of SST 0225, a Topical Ibuprofen Cream, in the Treatment of Pain Associated With Acute Ankle Sprain	Phase 3
Completed	`NCT01586390` - Functional Treatment for Acute Ankle Sprains: Softcast Wrap Versus MOKcast	Phase 2
Recruiting	`NCT06266520` - MNK Therapy in Releasing the Superficial Fascia for Patients With AAS: an Assessor-blinded, Randomised Controlled Trial	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT01874626 - Efficacy and Safety of SST 0225, a Topical Ibuprofen Cream, in the Treatment of Pain Associated With Acute Ankle Sprain

Phase 3

Completed

NCT01586390 - Functional Treatment for Acute Ankle Sprains: Softcast Wrap Versus MOKcast

Phase 2

Recruiting

NCT06266520 - MNK Therapy in Releasing the Superficial Fascia for Patients With AAS: an Assessor-blinded, Randomised Controlled Trial

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	NCT01272934
Study type	Interventional
Source	Novartis
Contact
Status	Completed
Phase	Phase 3
Start date	January 2011
Completion date	August 2011

Efficacy and Safety of Diclofenac Sodium Topical Gel 1% Applied Four Times Daily in Subjects With Acute Ankle Sprain

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms