NCT07408947

Brief Summary

Scorpion stings are a common medical emergency in Mexico, particularly in the state of Jalisco. While antivenom is the standard treatment for scorpion envenomation, there is variability in how it is used, including differences in dosing strategies. In addition, many patients use home remedies before seeking medical care, which may delay treatment and influence the severity of symptoms. This study is an observational, retrospective analysis of patients treated for scorpion envenomation in the emergency department of a public hospital in Jalisco, Mexico, between 2021 and 2023. Using information from medical records, the study examines the relationship between the use of home remedies, the time to receive medical care, clinical severity at presentation, and the antivenom dosing strategies used, including traditional and reduced-dose approaches. The goal of this study is to better understand factors associated with clinical severity and antivenom use in real-world emergency care. The results may help inform future clinical decision-making, promote rational use of antivenom, and improve timely access to appropriate medical treatment for patients with scorpion envenomation.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
3,145

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 7, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

January 15, 2026

Completed
29 days until next milestone

First Posted

Study publicly available on registry

February 13, 2026

Completed
Last Updated

February 13, 2026

Status Verified

February 1, 2026

Enrollment Period

4 months

First QC Date

January 15, 2026

Last Update Submit

February 6, 2026

Conditions

Keywords

antivenomscorpionhome remedyscorpionismscorpion envenomation

Outcome Measures

Primary Outcomes (1)

  • Clinical resolution of symptoms within 3 hours

    Proportion of patients with scorpion envenomation who achieved complete clinical resolution of signs and symptoms within three hours after initial medical management in the emergency department.

    From emergency department admission to 3 hours after initial treatment.

Secondary Outcomes (3)

  • Need for additional antivenom doses

    From initial antivenom administration until emergency department discharge (up to 24 hours)

  • Total number of antivenom vials administered

    From initial antivenom administration until emergency department discharge (up to 24 hours)

  • Use of supportive medications

    From initial antivenom administration until emergency department discharge (up to 24 hours)

Other Outcomes (3)

  • Clinical severity at presentation

    At emergency department triage (baseline)

  • Use of home remedies prior to medical care

    At emergency department triage (baseline)

  • Delay to medical care

    From time of scorpion sting to recorded emergency department triage time (baseline)

Study Arms (2)

Reduced dose

This group includes patients diagnosed with scorpion envenomation who were managed using a reduced-dose antivenom strategy during routine emergency care. In this approach, antivenom (faboterápico) was administered primarily to patients with systemic manifestations of envenomation. The initial dose generally consisted of a single intravenous vial, with additional vials administered only if clinical symptoms persisted or progressed after reassessment. Patients who did not receive antivenom because they presented without systemic symptoms were also included in this group. This management strategy differs from the Mexican national Clinical Practice Guidelines, which recommend antivenom administration to all patients with scorpion envenomation, regardless of the presence or absence of systemic symptoms. All treatment decisions were made by the treating physicians as part of standard clinical care, without protocol-mandated interventions.

Traditional dose

This group includes patients diagnosed with scorpion envenomation who were managed according to the traditional antivenom dosing strategy recommended by the Mexican national Clinical Practice Guidelines. These guidelines advise administering antivenom (faboterápico) to all patients with scorpion envenomation, independent of whether systemic symptoms are present, with dosing adjusted based on patient age and clinical severity. Under this strategy, patients typically received one or more intravenous vials of antivenom as an initial dose, with additional doses administered at predefined intervals if symptoms persisted, in accordance with guideline-based algorithms. All treatments were provided as part of routine emergency care, and no interventions were assigned for research purposes. This group reflects standard-of-care antivenom use in Mexico during the study period.

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients of all ages who presented with scorpion envenomation to the emergency department of a public hospital in Jalisco, Mexico, between 2021 and 2024. Patients were evaluated and treated as part of routine clinical care, following local clinical practice and national guidelines.

You may qualify if:

  • Patients of any age with a clinical diagnosis of scorpion envenomation.
  • Patients evaluated and treated in the emergency department of the participating hospital.
  • Availability of medical records with sufficient clinical information to assess envenomation severity, time to medical care, and antivenom administration.

You may not qualify if:

  • Patients with incomplete or missing medical records that do not allow determination of clinical severity or antivenom use.
  • Patients transferred from another healthcare facility after having already received definitive treatment for scorpion envenomation.
  • Patients with documented co-envenomation or alternative diagnoses that could confound clinical severity assessment.
  • Patients who declined medical evaluation or left the emergency department before completion of initial assessment and management.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centro Universitario de Ciencias de la Salud

Guadalajara, Jalisco, 44340, Mexico

Location

MeSH Terms

Conditions

Scorpion Stings

Condition Hierarchy (Ancestors)

Bites and StingsPoisoningChemically-Induced DisordersWounds and Injuries

Study Officials

  • Christian J Baños, PhD

    University of Guadalajara

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD

Study Record Dates

First Submitted

January 15, 2026

First Posted

February 13, 2026

Study Start

August 7, 2025

Primary Completion

December 1, 2025

Study Completion

December 31, 2025

Last Updated

February 13, 2026

Record last verified: 2026-02

Locations