CClinicalTrials.gg
Not yet recruitingNCT06228261PAT-HMARUpdated Jan 29, 2024

Critical Analysis of the Results in the Management of Penetrating Abdominal Trauma in the Past Fifteen Years.

An observational study in Penetrating Abdominal Trauma, sponsored by Hospital del Mar. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-01-29.

Sponsored by Hospital del Mar · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 9 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
1,000
Ages
18 Years and older
Sex
All
01

Study summary

Penetrating abdominal trauma (PAT) incidence varies between 3,1-12,8% and it comprises a wide range of injuries with varying patterns on diagnostic imaging. Last guidelines published in 2014 recommend the use of FAST and CXR as the Gold Standard method for evaluating. Computed Tomography (CT) is widely used in stable patients with PAT and it requires intravenous contrast and patient irradiation, leading to additional costs to healthcare services. This study aims to assess the management of PAT in our institution and with its results review the actual protocol.

Read the detailed description

Penetrating abdominal trauma (PAT) incidence varies between 3,1-12,8% and it comprises a wide range of injuries with varying patterns on diagnostic imaging. Last guidelines published in 2014 recommend the use of FAST and CXR as the Gold Standard method for evaluating. Computed Tomography (CT) is widely used in stable patients with PAT and it requires intravenous contrast and patient irradiation, leading to additional costs to healthcare services. This study aims to assess the management of PAT in our institution and with its results review the actual protocol.

A retrospective unicentric study will be conducted on a prospective database of stab wounds at the Department of General Surgery of Hospital del Mar over a 15-year period. The normality of the distribution of quantitative variables will be assessed using the Kolmogorov-Smirnov test. Comparison between qualitative variable groups will be performed using the Chi-square test or Fisher's exact test when appropriate, and non-parametric tests like the Mann-Whitney U test will be used to evaluate the significance of differences in means of quantitative variables. The odds ratios (OR) of predictor variables with outcome variables will be determined.

02

Conditions studied

  • Penetrating Abdominal Trauma

Keywords

  • Penetrating Trauma
  • Trauma surgery
  • Explorative laparoscopy
  • Trauma laparotomy
  • eFAST
03

In context

Wounds and Injuries

5,056 studies on the registry are indexed under Wounds and Injuries; 861 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 135 across 1,597 observational studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

Hospital del Mar is the lead sponsor of 45 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with a penetrating trauma in the neck admitted in Hospital del Mar from 2008 to 2023.

Inclusion criteria

  • All penetrating trauma patients admitted in the emergency department.

Exclusion criteria

Exclusion Criteria:

  • All patients with any other diagnostic different from penetrating trauma
  • Blunt trauma patients admitted in the emergency department
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
1,000 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Complications

    The main outcome measure was the total of complications in patients with a penetrating abdominal trauma assessed by the Clavien-Dindo Classification.

    Time frame: 2008-2023

  2. Mortality

    The second main outcome measure was the total of deaths in patients with a penetrating abdominal trauma assessed by preventable or non-preventable deaths.

    Time frame: 2008-2023

Secondary outcomes

  1. Explorations

    To describe the explorations that has been ordered: eFAST, CT Scan, explorative laparoscopy or laparotomy.

    Time frame: 2008-2023

  2. Demographyc description

    Description of the age and gender (Male / Female)

    Time frame: 2008-2023

  3. Physiologic description

    Description of the vitals at arrival (bates per minute, blood pressure)

    Time frame: 2008-2023

  4. Wound and abdominal exploration

    Description of the wound: bleeding, longitude, number of wounds and the abdominal explorations: peritonism or no peritonism.

    Time frame: 2008-2023

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 29, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06228261
Lead sponsor
Hospital del Mar
Responsible party
Ana María González Castillo (Doctor, Hospital del Mar) — Principal investigator
First posted
Jan 29, 2024
Start date
Mar 15, 2024 (estimated)
Primary completion
Dec 15, 2024 (estimated)
Completion
Mar 15, 2025 (estimated)
Last update
Jan 29, 2024

Study contacts

Ana María González Castillo, PhD
Contact
amgonzalezcastillo@gmail.com
+34665126866
Ana María González Castillo, PhD
principal investigator · Hospital del Mar

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion