Trial · NCT04413799
PVB vs Ketamine/Lidocaine in Rib Fracture Patients
NCT04413799, Early phase 1, Terminated, George Washington University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. PVB vs Ketamine/Lidocaine in Rib Fracture Patients. Trials, record NCT04413799. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04413799
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- PVB vs Ketamine/Lidocaine in Rib Fracture Patients
- NCT number
- NCT04413799
- Status
- Terminated
- Phases
- Early phase 1
- Enrollment
- 32 participants, actual
- Lead sponsor
- George Washington University
- Conditions
- Rib Fractures, Rib Trauma, Rib Fracture Multiple, Pain, Acute
- Interventions
- lidocaine, ketamine intravenous infusion, paravertebral block with ropivicaine
- First posted
- 2020-06-04
- Last updated
- 2025-06-22
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Numeric Pain Score (NPS) | throughout patients' hospitalization time, an average of 1 week | Numeric pain score is a scale of 1- 10 to ascertain patient's subjective pain severity. Patients will be asked their NPS daily. |
| Primary | Oral Morphine Equivalence (OME) | throughout patients' hospitalization time, an average of 1 week | Oral morphine equivalence is used to standardized the amount of opioid patient is using regardless the type of opioid that the patient is prescribed. |
| Secondary | Hospital Length of Stay (LOS) | captured after patient is discharged, an average of 1 week | The hospital length of stay will be captured after patient is discharged from the hospital. |
| Secondary | ICU Length of Stay (ICU LOS) | captured after patient is discharged, an average of 1 week | The ICU length of stay will be captured after patient is discharged from the hospital. |
| Secondary | incidence of pneumonia | throughout patients' hospitalization time, an average of 1 week | The diagnosis of pneumonia is captured when it is diagnosed by the primary team taking care of the patient. |
| Secondary | ventilator days | throughout patients' hospitalization time, an average of 1 week | We will obtain the number of days patient is on the ventilator |
| Secondary | disposition upon discharge | captured after patient is discharged, an average of 1 week | Patient's disposition after discharge will be recorded. Disposition of patient will be recorded as home, long term acute facility, skilled nursing facility or acute rehab |
| Secondary | in-hospital mortality | captured after patient is discharged, an average of 1 week | Patient's death will be recorded if it happen before discharge |
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.
Papers16
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/NCT04413799
GET https://conductscience.org/api/trials/v1/NCT04413799/registered