Trial · NCT07887516
Nerve Block Resolution Time Display and Pain Complaints
NCT07887516, Not applicable, Not yet recruiting, Medical University of South Carolina
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Nerve Block Resolution Time Display and Pain Complaints. Trials, record NCT07887516. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07887516
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Nerve Block Resolution Time Display and Pain Complaints
- NCT number
- NCT07887516
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 128 participants, estimated
- Lead sponsor
- Medical University of South Carolina
- Conditions
- Postoperative Pain, Rebound Pain, Fracture
- Interventions
- Physical display
- First posted
- 2026-10-21
- Last updated
- 2026-10-21
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Rate of postoperative pain-related complaints in each group | From time of nerve block administration until the time of first documented pain-related phone call or 48 hours from nerve block administration, whichever came first. | To evaluate whether physically displaying the expected nerve block resolution time on patients' splints reduces the rate of postoperative pain-related complaints. The rate will be measured as the percentage of patients in each study group who initiate at least 1 pain-related phone call within 48 hours of nerve block administration. Pain-related phone calls will be identified through patient chart review up to 48 hours after nerve block administration. Data will be compared between the interventional and control groups. The unit of measurement will be percentage of patients. |
| Secondary | Age and postoperative pain-related complaints | From time of enrollment until the time of first documented pain-related phone call or 48 hours from nerve block administration, whichever came first. | To evaluate the correlation between patient age and the rate of postoperative pain-related complaints. Age will be obtained by chart review and measured in years. The rate of postoperative pain-related complaints will be calculated as the percentage of patients within each age group who initiate at least 1 pain-related phone call within 48 hours of nerve block administration. Pain-related phone calls will be identified through patient chart review up to 48 hours after nerve block administration. |
| Secondary | Sex and postoperative pain-related complaints | From time of enrollment until the time of first documented pain-related phone call or 48 hours from nerve block administration, whichever came first | To evaluate the correlation between patient sex and the rate of postoperative pain-related complaints. Sex will be obtained by chart review and recorded as a categorical variable. The rate of postoperative pain-related complaints will be calculated as the percentage of patients within each sex who initiate at least 1 pain-related phone call within 48 hours of nerve block administration. Pain-related phone calls will be identified through patient chart review up to 48 hours after nerve block administration. |
| Secondary | Race and postoperative pain-related complaints | From time of enrollment until the time of first documented pain-related phone call or 48 hours from nerve block administration, whichever came first | To evaluate the correlation between patient race and the rate of postoperative pain-related complaints. Race will be obtained by chart review and recorded as a categorical variable. The rate of postoperative pain-related complaints will be calculated as the percentage of patients within each race who initiate at least 1 pain-related phone call within 48 hours of nerve block administration. Pain-related phone calls will be identified through patient chart review up to 48 hours after nerve block administration. |
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.
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.
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/NCT07887516
GET https://conductscience.org/api/trials/v1/NCT07887516/registered