Last reviewed · How we verify
NCT00869063: WIND
A Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of a Diclofenac Sodium Patch for the Topical Treatment of Acute Pain Due to Mild to Moderate Wrist Sprain, Strain or Contusion
Phase 3 trial testing Diclofenac Sodium Patch in Acute Pain in 214 participants. Completed in 1 September 2009.
1 July 2009
Quick facts
| Lead sponsor | Cerimon Pharmaceuticals |
|---|---|
| Phase | Phase 3 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 214 |
| Start date | 1 February 2009 |
| Primary completion | 1 July 2009 |
| Estimated completion | 1 September 2009 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Diclofenac Sodium Patch
- Matching Placebo Patch
Conditions studied
- Acute Pain — all drugs for Acute Pain →
Sponsor
Cerimon Pharmaceuticals
Who can join
Adults 17 to 75, any sex, with Acute Pain. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Change in average pain during daily activity
Time frame: Day 3
Sponsor's own description
The purpose of the study is to assess the effectiveness of once daily application of a diclofenac sodium topical patch in reducing acute pain due to mild to moderate wrist sprain, strain or contusion when applied to the painful area.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Topical NSAIDs for acute musculoskeletal pain in adults.
Derry S, Moore RA, Gaskell H, McIntyre M, et al · · 2015 · cited 74× · PMID 26068955 · DOI 10.1002/14651858.cd007402.pub3
Verify or expand the search:
- PubMed search for NCT00869063
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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- NCT07348523 — Comparison of the Postoperative Analgesic Efficacy of Classical and Modified Erector Spinae Plane Blocks After Lumbar Sp · NA · recruiting
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00869063 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Cerimon Pharmaceuticals
- Last refreshed: 26 January 2010
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00869063.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing