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Intraarticular Steroids, Saline and Occupational Therapy in People With CMC1 Osteoarthritis

Study acronym: PICASSO
StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Primary completion date: Sep 2026 to Jan 2027v7 Show 4 more changesShow less
    • Study completion date: Jun 2028 to Oct 2028
    • Eligibility criteria expanded, about 11 words
    • Secondary endpoints: details revised at 9 of 29 entries
    • Site details revised at 1 of 6 sites
  2. Primary completion date: Apr 2027 to Sep 2026
    • Study completion date: Nov 2028 to Jun 2028
    v6
  3. Re-verified, no change to tracked fieldsv5
  4. Primary completion date: Apr 2026 to Apr 2027
    • Study completion date: Nov 2027 to Nov 2028
    v4
  5. Primary endpoint revised
    • Eligibility criteria expanded, about 10 words
    • Secondary endpoints: 27 to 29
    • Site details revised at 3 of 6 sites
    v3
  6. Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Study sites: 0 to 6
    • Primary completion date: Oct 2025 to Apr 2026
    • Study completion date: Oct 2027 to Nov 2027
    • Start date changed from estimate of Oct 2023 to Nov 3, 2023
  7. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
A placebo-controlled randomized controlled trial exploring the effect of intraarticular steroids, saline or an occupational therapy intervention in inflammatory carpometacarpal-1 osteoarthritis
Trial Details
NCT Number NCT06084364
Lead Sponsor Diakonhjemmet Hospital
Collaborators: Vestre Viken Hospital Trust, Helse Stavanger HF, Haugesund Rheumatism Hospital, St. Olavs Hospital, Nordlandssykehuset HF
Conditions
(from sponsor)		 Osteoarthritis Thumb
Related terms Inflammation, Osteoarthritis, Pain
Enrollment 354 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov