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Trial · NCT06669000

Time Required to Dissolve Urate Deposits

NCT06669000, Recruiting, Assistance Publique - Hôpitaux de Paris

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Time Required to Dissolve Urate Deposits. Trials, record NCT06669000. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06669000

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Time Required to Dissolve Urate Deposits
NCT number
NCT06669000
Status
Recruiting
Enrollment
250 participants, estimated
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Conditions
Gout
Interventions
Standard X-Rays, Ultrasound, DECT of feet, DNA sample, Serum collection
First posted
2024-11-01
Last updated
2026-02-19

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTime required for complete dissolution of urate depositsChange between baseline (month 0) and up to 48 months after initiation of ULT
For each patient, urate deposit dissolution will be monitored by repeated US scans. The US features which will be recorded according to the Outcome Measures in Rheumatology (OMERACT) scoring system: * at MTP1s: the DC sign, tophi and aggregates * at the knees (femoral condyles): the DC sign. The aggregates will only be scored if the DC sign and/or tophus are present and if the aggregates are not located inside a tophus. For each site, the US features will be graded as follows: absent (0) possible (1) moderate (2) important (3). Thus, a score (0-24) will be calculated for each patient. A score of 0 means that there are no longer urate deposits, while a score of 24 means that there are a lot of urate deposits. Dissolution is considered to have been achieved when a score of 0/24 is reached on two successive US scans performed 6 months apart
SecondaryNumber of flaresAt Month 0, Month 6, Month 12, Month 18, Month 24, Month 30, Month 36, Month 48
Flares is defined when 3 of the following 4 criteria are present: * Patient-defined flare * Pain at rest greater than 3 on a 0-10 point numerical rating scale. * Presence of at least one swollen joint. * Presence of at least one hot joint.
SecondaryHealth status as assessed by the EQ-5D-3L questionnaireAt Month 0, Month 6, Month 12, Month 24, Month 36, Month 48
Health status as assessed by the EQ-5D-3L descriptive system comprising the following five dimensions: * Mobility, * Self-care, * Usual activities, * Pain/discomfort * Anxiety/depression. Each dimension has 3 levels: no problems, some problems, and extreme problems. The patient is asked to indicate his/her health state by ticking the most appropriate box. This decision results into a 1-digit number. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.
SecondaryPatient self-rated health on a vertical visual analogue scale (EQ VAS)At Month 0, Month 6, Month 12, Month 24, Month 36, Month 48The EQ VAS records the patient's self-rated health on a vertical visual analogue scale from 0 to 100, with 100 being the best health and 0 corresponding to the worst health.
SecondaryHealth status as assessed by the HAQ-ID questionnaireAt Month 0, Month 6, Month 12, Month 24, Month 36, Month 48
The questionnaire includes 8 sections: dressing, arising, eating, walking, hygiene, reach, grip, and activities, with 4 questions for each section. Scoring within each section is from 0 (without any difficulty) to 3 (unable to do). For each section the score given to that section is the worst score within the section. The 8 scores of the 8 sections are summed and divided by 8. The score obtained ranges from 0 to 3. The higher the score, the worse the state of health.
SecondaryProteins profilsMonth 0, Month 6, Month 24, Month 36Change in plasma Proteins concentrations

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT06669000

GET https://conductscience.org/api/trials/v1/NCT06669000/registered