Magnesium-Enhanced ESPB for Respiratory Recovery and Analgesia in Unilateral Rib Fractures
NCT07929402, Not applicable, Not yet recruiting, Assiut University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Magnesium-Enhanced ESPB for Respiratory Recovery and Analgesia in Unilateral Rib Fractures | ClinicalTrials.gov |
| NCT number | NCT07929402 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 36 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Assiut University | ClinicalTrials.gov |
| Conditions | Unilateral Rib Fracture, ESPB, MgSO4, Respiratory Recovery, Analgesic Efficacy | ClinicalTrials.gov |
| Interventions | Bupivacaine 0.25%, Magnesium sulfate 500 mg | ClinicalTrials.gov |
| First posted | 2026-11-10 | ClinicalTrials.gov |
| Last updated | 2026-11-10 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Diaphragmatic excursion | 24 hours | To compare the area under the curve of the change in ipsilateral diaphragmatic excursion from baseline over the first 24 hours after ultrasound-guided ESPB. Diaphragmatic excursion will be measured in centimeters . | ClinicalTrials.gov |
| Secondary | Incentive spirometry | 24 hour | volume will be assessed in the same position and by blinded assessor in milliliters | ClinicalTrials.gov |
| Secondary | Semiquantitative Cough Strength Score (SCSS) | 24 hours | No cough on command 0 Audible movement of air but no audible cough 1 Weakly (barely) audible cough 2 Clearly audible cough 3 Strong cough 4 Multiple sequential strong coughs 5 Higher means better | ClinicalTrials.gov |
| Secondary | Visual Analog Scale [VAS] scores | 24hours | at rest and during exertion No pain 0 Mild pain 1-3 Moderate pain 4-6 Severe pain 7-10 Higher means worse | ClinicalTrials.gov |
| Secondary | Time to first request for rescue analgesia | 24 hours | administered according to institutional pain management protocols if pain scores exceed specific thresholds will be measured in hours after the block | ClinicalTrials.gov |
| Secondary | Total cumulative dose of rescue analgesia | 24 hours | administered according to institutional pain management protocols if pain scores exceed specific thresholds will be measured in milligrams. | ClinicalTrials.gov |
| Secondary | Number of rescue analgesia boluses | 24 hours | administered according to institutional pain management protocols if pain scores exceed specific thresholds will be measured in milligrams. | ClinicalTrials.gov |
| Secondary | Patient satisfaction score | 24 hours | Very dissatisfied 1 Dissatisfied 2 Neutral 3 Satisfied 4 Very satisfied 5 Higher means better | 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 9
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)