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Completed

NCT Number: NCT05478642

Influence of Psychological Status on the Results of Pain Treatment in Patients With Gunshot and Mine-explosive Wounds

82.1% of patients with gunshot and mine-explosive wounds and wounds during hostilities in Ukraine have negative results of pain treatment, which leads to its chronicity. Examining the effect of psychological status on pain management outcomes in these patients may improve their treatment outcomes.

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Key information

Sex eligibility

Male

Study type

Observational

Primary location

Bogomolets National Medical University, Ministry of Health of Ukraine

Kyiv, Ukraine

About this study

The influence of the amount of damage and operative interventions on the results of pain treatment in patients with gunshot and mine-explosive wounds at the stages of treatment needs to be studied, because the subjective feelings and emotional experiences experienced by patients during the wounding in combat conditions through the prism of psychological disorders have its features. Since in 82.1% of cases it is not possible to achieve a positive result of treatment, the data of our study will play an important role in their treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • availability gunshot and mine-explosive wounds

Exclusion criteria

  • absence gunshot and mine-explosive wounds

Treatment and study plan

The Hospital Anxiety and Depression Scale.

Other

The study was carried out on the basis of the National Military Medical Clinical Center "Main Military Clinical Hospital". All patients participated in Operation Joint Forces and received gunshot wounds during combat operations.

A retrospective analysis of disease histories for the period from 2014 to 2021 was carried out. Data collection was carried out at all stages of treatment: medical and nursing brigade, military mobile hospital, military medical clinical center, during rehabilitation, within 12 months of the injury.

Recruitment of patients for the prospective study was carried out in the period from 02.24.2022 to 05.24.2022. Data collection was carried out during the Russian invasion of Ukraine and the offensive on Kyiv.

Other names: Mississippi PTSD scale (military version), Chaban Quality of Life Scale

Primary outcomes

  1. visual analog scale

    Time frame: 12 months

    evaluation of the number of points

  2. Didier Bouhassiraa DN4

    Time frame: 12 months

    evaluation of the number of points

  3. The Hospital Anxiety and Depression Scale

    Time frame: 12 months

    evaluation of the number of points

  4. Chaban Quality of Life Scale

    Time frame: 12 months

    evaluation of the number of points

  5. Mississippi PTSD scale (military version)

    Time frame: 12 months

    evaluation of the number of points

Sponsors and collaborators

Lead sponsor

Bogomolets National Medical University

Other

Registry information

Acronym: IPSRPTPGaM-EW

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jul 28, 2022
Registry last updated
Aug 1, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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