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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05478668
Other study ID # ?158, 2022.23.05
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 24, 2022
Est. completion date May 24, 2022

Study information

Verified date July 2022
Source Bogomolets National Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

82.1% of patients with gunshot and mine-explosive wounds during hostilities in Ukraine have negative results of pain treatment, which leads to its chronicity. Identifying predictors of pain chronicity in these patients may improve their treatment outcomes.


Description:

The study of predictors of pain chronicity in patients with gunshot and mine-explosive wounds requires in-depth study, because the subjective feelings and emotional experiences experienced by patients during the wounding in combat conditions have their own characteristics. Since pain becomes chronic in 82.1%, the data of our study will play an important role in preventing the chronicity of pain.


Recruitment information / eligibility

Status Completed
Enrollment 2215
Est. completion date May 24, 2022
Est. primary completion date May 24, 2022
Accepts healthy volunteers No
Gender Male
Age group N/A and older
Eligibility Inclusion Criteria: - the presence of gunshot and mine-explosive injuries Exclusion Criteria: - absence of gunshot and mine-explosive injuries

Study Design


Related Conditions & MeSH terms


Intervention

Other:
visual analog scale
In all patients, the assessment of anesthetic risk was carried out according to the ASA scale. The basic tool for pain intensity research was a visual analog scale. Intervals between analgesia were also studied. The study of the neuropathic component of pain was carried out using the Didier Bouhassiraa neuropathic pain diagnostic questionnaire. Study of the presence of an acute stress reaction The Hospital Anxiety and Depression Scale. Research on the presence of post-traumatic stress disorders was carried out using the Mississippi scale of post-traumatic stress disorders (military version). Satisfaction with treatment results was studied using the Chaban Quality of Life Scale.

Locations

Country Name City State
Ukraine Bogomolets National Medical University, Ministry of Health of Ukraine Kyiv

Sponsors (1)

Lead Sponsor Collaborator
Bogomolets National Medical University

Country where clinical trial is conducted

Ukraine, 

Outcome

Type Measure Description Time frame Safety issue
Primary visual analog scale evaluation of the number of points 1 year
Primary Didier Bouhassiraa DN4 evaluation of the number of points 1 year
Primary The Hospital Anxiety and Depression Scale evaluation of the number of points 1 year
Primary Chaban Quality of Life Scale evaluation of the number of points 1 year
Primary Mississippi PTSD scale (military version) evaluation of the number of points 1 year
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