Phase 2 Osteoarthritis Trial, Recruiting NCT06237153 Sponsor: Marie Badalamente Condition: Osteoarthritis
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Phase 2 Osteoarthritis Trial, Recruiting

NCT06237153
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are male or female and older than 18 years of age.
  • People who have been diagnosed with thumb base (CMC) joint arthritis at stage I, II, or III, confirmed by X-ray.
  • People whose thumb pain is rated 5 or higher on a standard 10-point pain scale.
  • People who are willing and able to give written consent and follow the study requirements.
  • People who are willing to avoid using opioid pain medications and over-the-counter pain medications during the study, and to keep a log if they do use them.

Who may not be able to join:

  • People who are pregnant, breastfeeding, planning to become pregnant during the study, or unwilling to use birth control during the study.
  • People with any condition or abnormality that, in the trial doctor's opinion, could affect their safety or the reliability of study results.
  • People with a known or suspected allergy to the study drug (TA-ER) or its ingredients, including triamcinolone acetonide.
  • People with stage IV CMC joint arthritis, as these cases typically involve severe joint damage and are more likely to require surgery.
  • People who have been diagnosed with rheumatoid arthritis, septic arthritis, gout-related arthritis, psoriatic arthritis, thumb joint fluid buildup, DeQuervain's disease, or trigger thumb.
  • People who have previously had surgery to reconstruct the affected thumb joint.
  • People with serious, uncontrolled long-term medical conditions.
  • People who have received hyaluronan or platelet-rich plasma (PRP) injections into the affected thumb joint within the past 6 months.
  • People who have received a steroid injection into the affected thumb joint within the past 3 months.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 12 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Marie Badalamente
Registry
ClinicalTrials.gov
Start date
21 November 2023
Est. completion
31 December 2025

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Visual Analog Pain Score

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov