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Abdominal InjuriesDIRECTNCT07330349

Alcohol, Psychoactive Drugs, Analgesics and Evaluation in Penetrating Abdominal Trauma

An observational study of Abdominal Injuries and Alcohol Intoxication, run by Fundacion Clinica Valle del Lili at 2 sites in Colombia.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This prospective observational study aims to evaluate whether alcohol consumption, psychoactive drug use, or prior administration of analgesics affects the clinical evaluation and surgical decision-making process in patients with penetrating abdominal trauma. Read more about this study

Who is it for?
Ages 15 years and older
What is being tested?
Alcohol consumption, Psychoactive substance use and Analgesic administration
How many people
363 participants
Where
2 sitesColombia
Study dates
25 Nov 2020to 30 Jan 2026
How long will I take part?
28 Days
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: The study population includes patients aged 14 years and older presenting with penetrating abdominal trauma to two university-affiliated trauma centers in Cali, Colombia (one public and one private). Patients are evaluated and managed according to standard trauma care protocols, including immediate operative management or clinical observation with serial physical examination, as clinically indicated. The study assesses the impact of alcohol consumption, psychoactive substance use, and analgesic administration on the clinical evaluation process and surgical decision-making during hospitalization.

Who may be able to join

  • Patients presenting to the emergency department with penetrating abdominal trauma.
  • Age 14 years or older.
  • Patients evaluated and managed according to standard trauma care protocols, including immediate operative management or clinical observation with serial physical examination, as clinically indicated.
  • Patients admitted to the participating trauma centers during the study period.

Who cannot join

  • Patients transferred from another institution after initial surgical intervention.
  • Patients declared dead on arrival.
  • Patients with incomplete or missing clinical data precluding assessment of outcomes of interest.

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Sergio I Prada Ríos, PhD contact

+57 6023319090 ext. 4380

sergio.prada@fvl.org.co

Alberto F García, MD, MSc contact

+57 3154676870

alberto.garcia@fvl.org.co

Colombia2 sites, 2 recruiting
  • Fundación Valle del Lili

    Cali, Valle del Cauca Department

    Alberto F García, MD, MSc, +57 3154676870, alberto.garcia@fvl.org.co

    Recruiting
  • Hospital Universitario del Valle Evaristo García

    Cali, Valle del Cauca Department

    Adolfo González, MD, +57 3162896406, adolfo.gonzalez@correounivalle.edu.co

    Recruiting

Other trials in Colombia

About this study

Official title: Influence of Alcohol, Psychoactive Drugs, and Analgesic Administration on the Evaluation Process in Patients With Penetrating Abdominal Trauma

This prospective observational study aims to evaluate whether alcohol consumption, psychoactive drug use, or prior administration of analgesics affects the clinical evaluation and surgical decision-making process in patients with penetrating abdominal trauma.

The study will be conducted in two level I trauma centers in Cali, Colombia: a public university hospital and a private university hospital, both with high volumes of trauma patients and established protocols for non-operative management using serial physical examination.

Read more

In many trauma centers, serial physical examination is used to safely identify patients who require surgical intervention. However, there is concern that intoxication or altered mental status may reduce the reliability of physical examination, potentially leading to unnecessary imaging studies, delays in surgical decision-making, or non-therapeutic laparotomies. Despite this concern, available evidence supporting these assumptions is limited.

Patients older than 14 years with penetrating abdominal trauma who undergo clinical evaluation to decide on surgical intervention. Patients will be classified according to the presence or absence of alcohol consumption, psychoactive substance use, or prior analgesic administration. The primary outcome is the time from hospital admission to the decision for surgical intervention. Secondary outcomes include trauma severity, need for surgery, length of hospital and intensive care unit stay, complications, and mortality.

By comparing patients with and without substance exposure across two different trauma care settings, this study seeks to determine whether serial physical examination remains a reliable and safe method for clinical decision-making in this population. The results may help optimize evaluation strategies, reduce unnecessary surgical procedures and diagnostic tests, and improve the standardization of care for patients with penetrating abdominal trauma.

Read the detailed description

This is a prospective observational cohort study designed to evaluate the impact of alcohol consumption, psychoactive drug use, and prior administration of analgesics on the clinical evaluation process and surgical decision-making in patients with penetrating abdominal trauma.

The study will be conducted at two level I trauma centers in Cali, Colombia: one public university hospital and one private university hospital. Both institutions manage a high volume of trauma patients and apply standardized protocols based on serial physical examination for the evaluation of patients with penetrating abdominal trauma.

Patients older than 14 years who present with penetrating abdominal trauma and are hemodynamically stable will be evaluated according to routine institutional protocols, including serial abdominal physical examinations and selective use of diagnostic adjuncts such as focused abdominal sonography for trauma (FAST) or computed tomography, when clinically indicated. No additional diagnostic or therapeutic interventions will be performed as part of the study.

The exposure of interest is the presence of alcohol consumption, psychoactive substance use, or prior administration of analgesics before or during the initial clinical evaluation. These exposures will be identified through clinical assessment and medical record review and will be categorized according to predefined operational definitions.

The primary analytical focus is the interval between hospital admission and the decision for surgical intervention. Secondary analyses will explore associations between substance exposure and trauma severity, need for operative management, length of hospital stay, intensive care unit admission and length of stay, postoperative complications, and in-hospital mortality.

Data will be collected prospectively using standardized electronic case report forms. Data quality will be ensured through predefined range checks, consistency rules, and periodic review of entered data by the study investigators. Source data verification will be performed by comparing selected registry variables with information documented in the medical records.

Sample size was estimated to detect a clinically relevant difference in time to surgical decision between exposed and non-exposed patients, assuming an alpha level of 0.05, a statistical power of 80%, and an expected hazard ratio of 0.7. Based on the anticipated probability of requiring laparotomy of 0.68, a total of 247 events (laparotomies) were required, corresponding to 363 patients, to ensure an adequate number of events for time-to-event analysis.

Statistical analysis will include descriptive summaries of baseline characteristics, comparison of categorical variables using chi-square or Fisher's exact tests, and comparison of continuous variables using parametric or non-parametric methods as appropriate. Time-to-event analyses will be performed using Cox proportional hazards regression models, adjusting for relevant covariates such as age, sex, mechanism of injury, trauma severity, and type of substance exposure.

This study is observational and involves minimal risk to participants, as all evaluations and management decisions are part of standard clinical care. The results are expected to provide evidence regarding the reliability of serial physical examination in patients with penetrating abdominal trauma who present under the influence of alcohol, psychoactive substances, or analgesics, and may contribute to improving and standardizing trauma evaluation protocols across different clinical settings.

Being tested
Alcohol consumption, Psychoactive substance use, Analgesic administration
Keywords
Trauma decision making, Time to surgery, Penetrating abdominal trauma, Alcohol use, Psychoactive substances, Analgesic administration
Medical subject headings
Abdominal Injuries, Alcoholic Intoxication, Substance-Related Disorders, Alcohol Drinking

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Alcohol consumptionOther

    Alcohol consumption prior to hospital admission, identified through patient report, clinical assessment, or laboratory testing when available, and observed as part of routine trauma care, not assigned by the study.

  • Psychoactive substance useOther

    Use of psychoactive substances prior to hospital admission, identified through clinical history, physical examination, or toxicology screening when available, and observed without modification by the study protocol.

  • Analgesic administrationOther

    Administration of analgesic medications prior to or during initial hospital evaluation as part of standard trauma care, not assigned, standardized, or modified by the study.

Study groups in NCT07330349
Study groupRoleWhat they receive
Patients with Penetrating Abdominal TraumaPatients presenting with penetrating abdominal trauma who are evaluated and managed according to standard trauma care protocols, including immediate operative management or clinical observation with serial physical examination, as clinically indicated.
Receives: Other: Alcohol consumption; Other: Psychoactive substance use; Other: Analgesic administration

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Time to surgical decision

    Time elapsed from hospital admission to the clinical decision to proceed with surgical intervention, measured in hours, based on standard trauma care assessment.

    Measured: Up to 28 days

Secondary outcomes (5)
  1. Need for surgical intervention

    Requirement of operative management during hospital stay.

    Measured: Up to 28 days

  2. Time to surgery

    Time elapsed from hospital admission to the start of surgical intervention, measured in hours.

    Measured: Up to 28 days

  3. In-hospital mortality

    Death occurring during the index hospitalization.

    Measured: During hospitalization (Up to 28 days)

  4. Trauma severity

    Trauma severity will be assessed using ATI (Abdominal trauma index).

    Measured: 28 Days

  5. Intraoperative bleeding

    Intraoperative bleeding will be assessed by estimating total blood loss during the surgical procedure described by surgeon.

    Measured: 28 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Jan 2026
  2. Study start25 Nov 2020
  3. Primary completion24 Dec 2025
  4. Study completion30 Jan 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
363 participants (estimated)
Target duration
28 Days
IDs, dates and publications
ClinicalTrials.gov ID
NCT07330349
Sponsor's protocol ID
2020.1639
Acronym
DIRECT
Status last verified
Dec 2025
First submitted
29 Dec 2025
Last updated
9 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Abdominal Injuries and Alcohol Intoxication, run by Fundacion Clinica Valle del Lili at 2 sites in Colombia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 9 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Colombia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Sergio I Prada Ríos, PhD (+57 6023319090 ext. 4380, sergio.prada@fvl.org.co), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Time to surgical decision (time frame: Up to 28 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jan 2026.

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