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Completed

NCT Number: NCT05478655

Predictors of Treatment Failure Pain Among Patients With Mine-explosive Wounds

Mine-explosive wounds in the general structure of combat sanitary losses reach 25%. They are characterized by significant damage resulting in high intensity pain. In patients who received mine-explosive injuries in the conditions of hostilities, such pain has its own unique features. It is necessary to pay more attention to the problem of pain treatment in patients of this category, because about 87.2% of cases have negative results of treatment - it becomes chronic.

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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 peculiarities of pain in patients with mine-explosive wounds depending on the localization of the wound at the stages of treatment need 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 their own characteristics. Since in 87.2% 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

  • chronic pain, mine-explosive wounds

Exclusion criteria

  • absence of mine-explosive wounds

Treatment and study plan

Visual analog scale

Other

VAS was studied: 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 and further 1, 3, 6, 12 months after the injury; 5) at the rehabilitation stage. Intervals between analgesia were also studied.

Other names: neuropathic pain Didier Bouhassiraa, Nadine Attala et al. Pain, 2005, 114: 29-36 (DN4)., ASA, The Hospital Anxiety and Depression Scale, 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

Sponsors and collaborators

Lead sponsor

Bogomolets National Medical University

Other

Registry information

Acronym: PTFPAPM-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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