Trial · NCT06040840
WALANT Versus Axillary Brachial Plexus Block in Carpal Tunnel Release
NCT06040840, Not applicable, Completed, CMC Ambroise Paré
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. WALANT Versus Axillary Brachial Plexus Block in Carpal Tunnel Release. Trials, record NCT06040840. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06040840
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- WALANT Versus Axillary Brachial Plexus Block in Carpal Tunnel Release
- NCT number
- NCT06040840
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 130 participants, actual
- Lead sponsor
- CMC Ambroise Paré
- Conditions
- Carpal Tunnel Syndrome
- Interventions
- BAX, Tourniquet, Lidocaine, WALANT, Lidocaine + Epinephrine
- First posted
- 2023-09-18
- Last updated
- 2026-04-08
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Regional anesthesia success | 2 hours | Need (or not) for additional anesthetic procedure during surgery: analgesics, sedation, general anesthesia, local anesthetics |
| Secondary | Surgery duration | 2 hours | Time (in minutes) between the skin incision and the wound dressing procedure. |
| Secondary | Length of hospital stay | 24 hours | Time (in minutes) between ward admission and discharge. |
| Secondary | Discharge criteria assessed by PADSS | 24 hours | Time (in minutes) between the regional anesthesia and the ability to discharge defined by the modified Post Anesthesia Discharge Scoring System (PADSS) who achieve a score of 9 or more. |
| Secondary | Patient satisfaction assessed by EVAN-LR self-reported questionnaire | 24 hours | EVAN-LR self-reported questionnaire comprising 19 items structured in five dimensions, depending on their content: Attention (4 items), Information (5 items), Discomfort (4 items), Waiting (2 items), and Pain (4 items). Each item is linearly transformed to a 0-100 scale, with 100 indicating the best possible level of satisfaction and 0 the worst. |
| Secondary | Postoperative pain at the surgical site assessed by VRS | 24 hours | Maximum postoperative pain at the surgical site will be assessed at Day-0 et at Day-1 using a Verbal Rating Scale (VRS) ranging from 0 to 10 (0=no pain, 10=worst possible pain). |
| Secondary | Surgical site bleeding | 2 hours | Surgeon's clear-field satisfactory score: 1=bloodless, 2=little blood, 3=bloody field but performable, 4=bloody field |
| Secondary | Rate of complications | 24 hours | Incidence of complications related to RA procedure: vascular puncture, paresthesia, local anesthetic systemic toxicity |
Source ClinicalTrials.gov
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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 41233154 | RESULT |
Source PubMed
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.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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/NCT06040840
GET https://conductscience.org/api/trials/v1/NCT06040840/registered