Trial · NCT06917118
Multimodal Pain Management After Wide Awake Local Anesthesia No Tourniquet Orthopedic Hand Surgery: A Randomized Control Trial
NCT06917118, Not applicable, Not yet recruiting, University of Puerto Rico
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Multimodal Pain Management After Wide Awake Local Anesthesia No Tourniquet Orthopedic Hand Surgery: A Randomized Control Trial. Trials, record NCT06917118. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06917118
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Multimodal Pain Management After Wide Awake Local Anesthesia No Tourniquet Orthopedic Hand Surgery: A Randomized Control Trial
- NCT number
- NCT06917118
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 100 participants, estimated
- Lead sponsor
- University of Puerto Rico
- Conditions
- Pain Management
- Interventions
- Oxycodone 5mg taken first, Acetaminophen, Naproxen Tablets, 500 mg, OxyCODONE 5 mg Oral Tablet
- First posted
- 2025-04-08
- Last updated
- 2025-04-08
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | VAS Pain Scores | From enrollment to the end of treatment at 7 days | VAS pain scores will be assessed using a patient- completed VAS pain questionnaire until 7 days post-op. Patients will take the questionnaire home and report pain scores in the morning and in the afternoon every day for a week. |
| Primary | Patient Satisfaction | From enrollment to the end of treatment at 7 days | Patient satisfaction will be assessed using the Patient Satisfaction Questionnaire Short Form (PSQ-18) |
| Primary | Total Opioid Usage | From enrollment to the end of treatment at 7 days | Will be reported in as morphine milligram equivalents (MMEs) |
| Secondary | Breakthrough Pain | From enrollment to the end of treatment at 7 days | Breakthrough pain will be reported as a binary outcome (Y/N) |
| Secondary | Length of Treatment | From enrollment to the end of treatment at 7 days | Patients will be asked to report the number of days in which they used the provided pain control treatment |
| Secondary | Indication for WALANT surgery | From enrollment to the end of treatment at 7 days | We will report the indication for treatment for each patient to include in the final analysis |
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.
Papers20
The papers the trial lists on ClinicalTrials.gov.
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/NCT06917118
GET https://conductscience.org/api/trials/v1/NCT06917118/registered