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Predictors of Treatment Failure Pain Among Patients Gunshot Wounds

NCT05482061 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2215

Last updated 2022-08-01

No results posted yet for this study

Summary

In patients with gunshot wounds during hostilities in Ukraine, 76.9% have negative results of pain treatment, which leads to its chronicity. Identifying predictors of negative pain outcomes in these patients may improve their treatment outcomes.

Conditions

Interventions

OTHER

visual analog scale (VAS).

The basic tool for pain intensity research was the VAS: 1) before and after anesthesia - at the stage of the medical and nursing brigade, military mobile hospital, military medical clinical center; 2) at the stage of the medical and nursing team - within 2 days; 3) at the stage of the military mobile hospital - within 5 days; 4) at the stage of the military medical clinical center - within 7 days, at the time of discharge from the hospital; 5) at the rehabilitation stage. Intervals between analgesia were also studied. The study of the neuropathic component of pain was carried out using the diagnostic DN4: military mobile hospital, a military medical clinical center, then at the time of discharge from a military medical clinical center. Study of the presence of an acute stress reaction - anamnesis + The Hospital Anxiety and Depression Scale. Satisfaction with treatment results was studied using the Chaban Quality of Life Scale.

Sponsors & Collaborators

  • Bogomolets National Medical University

    lead OTHER

Principal Investigators

  • Vasyl' Horoshko, PhD · Bogomolets National Medical University, Ministry of Health of Ukraine

Eligibility

Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-02-24
Primary Completion
2022-05-24
Completion
2022-05-24

Countries

  • Ukraine

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05482061 on ClinicalTrials.gov