Trial · NCT07911085
From Blast Injury to Multicompartment Dysfunction:
NCT07911085, Not yet recruiting, Ukrainian Society of Regional Anesthesia and Pain Therapy
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. From Blast Injury to Multicompartment Dysfunction:. Trials, record NCT07911085. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07911085
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- From Blast Injury to Multicompartment Dysfunction:
- NCT number
- NCT07911085
- Status
- Not yet recruiting
- Enrollment
- 100 participants, estimated
- Lead sponsor
- Ukrainian Society of Regional Anesthesia and Pain Therapy
- Conditions
Compartment Syndrome, Compartment Syndrome Nontraumatic Lower Extremity, Compartment Syndrome Traumatic Upper Extremity, Compartment Syndromes, Blast Injury, Abdominal Compartment Syndrome, Polycompartment Syndrome, Thoracic Compartment Syndrome
- First posted
- 2026-11-02
- Last updated
- 2026-11-02
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Proportion of Patients With Polycompartment Syndrome | From admission for the index blast injury; assessed at admission and during the first 3 hours, with in-hospital follow-up through Day 7 or until hospital discharge or in-hospital death, whichever occurs first | Number and percentage of patients meeting the study's prespecified definition of compartment syndrome or pressure-related dysfunction in two or more anatomical compartments (abdomen, thorax, cranium, and/or extremity). Cases will be classified as concurrent or sequential when timing is documented. |
| Secondary | Distribution of Affected Anatomical Compartments | From admission for the index blast injury; assessed at admission and during the first 3 hours, with in-hospital follow-up through Day 7 or until hospital discharge or in-hospital death, whichever occurs first | Frequency and percentage of patients with abdominal, thoracic, cranial, or extremity involvement, including documented combinations. |
| Secondary | Timing and Sequence of Compartment Involvement | From admission for the index blast injury; assessed at admission and during the first 3 hours, with in-hospital follow-up through Day 7 or until hospital discharge or in-hospital death, whichever occurs first | Proportion of cases with simultaneous versus sequential involvement and, where documented, the time between the first and subsequent compartment involvement. |
| Secondary | In-Hospital Clinical Outcomes | From admission for the index blast injury; assessed at admission and during the first 3 hours, with in-hospital follow-up through Day 7 or until hospital discharge or in-hospital death, whichever occurs first | In-hospital clinical outcomes will be obtained from the medical record and reported separately. These will include in-hospital mortality, hospital length of stay, ICU admission and ICU length of stay, need for mechanical ventilation, and documented complications. |
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/NCT07911085
GET https://conductscience.org/api/trials/v1/NCT07911085/registered