Conventional or Ultrasound Guided Puncture Technique for the Distal Radial Artery, Direct Comparison Study (Sound Distal Trial).
NCT07928960, Not applicable, Completed, CHU Helora Jolimont
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Conventional or Ultrasound Guided Puncture Technique for the Distal Radial Artery, Direct Comparison Study (Sound Distal Trial). | ClinicalTrials.gov |
| NCT number | NCT07928960 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 600 participants, actual | ClinicalTrials.gov |
| Lead sponsor | CHU Helora Jolimont | ClinicalTrials.gov |
| Conditions | Percutaneous Coronary Intervention | ClinicalTrials.gov |
| Interventions | echo guided puncture, conventional puncture | ClinicalTrials.gov |
| First posted | 2026-11-10 | ClinicalTrials.gov |
| Last updated | 2026-11-10 | ClinicalTrials.gov |
Registered outcomes 10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | first-wiring pass success rate | from starting procedure to end of procedure | ClinicalTrials.gov | |
| Secondary | total number of attempts | from starting procedure to end of procedure | The total number of attempts needed for the first-wiring pass success rate. Attempts will be defined as puncture of the artery, confirmed by the back-bleeding through the needle hub but withdrawal of the needle, after failing the wiring. | ClinicalTrials.gov |
| Secondary | time to access | from starting procedure to end of procedure | The time to access will be measured from the point of the first application of the operator's fingers or US probe to guide access to a successful first-wiring pass success rate. For the blind puncture group: the first application of the operator's fingers on the artery to palpate it. | ClinicalTrials.gov |
| Secondary | Bleeding | from starting procedure to end of procedure | Puncture site bleeding according to EASY criteria and Overall bleeding according to BARC criteria | ClinicalTrials.gov |
| Secondary | Successful sheath insertion | from starting procedure to end of procedure | ClinicalTrials.gov | |
| Secondary | crossover | from starting procedure to end of procedure | Crossover to US guidance and/or Access site cross-over | ClinicalTrials.gov |
| Secondary | Vascular access-site complication | from starting procedure to end of procedure | ClinicalTrials.gov | |
| Secondary | Distal radial artery occlusion | from starting procedure to discharge | ClinicalTrials.gov | |
| Secondary | Hemostasis time | from starting procedure to end of procedure | ClinicalTrials.gov | |
| Secondary | Pain associated with the procedure | from starting procedure to discharge | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 2
The papers the trial lists on ClinicalTrials.gov.
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)