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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03660150
Other study ID # CRC_GHN_2018_003
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2018
Est. completion date August 31, 2018

Study information

Verified date August 2018
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Massive burns are serious life-threatening conditions. Recent advances in their management now allow the survival of a growing number of patients. The burn care paradigm is transformed: the evaluation of survival at the end of acute care is no longer sufficient for a good evaluation of practices; the attention now focuses on long-term health-related quality of life (HR-QOL).The recently validated French translation of the burn specific health scale brief version makes this evaluation now feasible in French burn centers. The objectives of this study are to evaluate the HR-QOL of massive burn survivors, to compare it to another chronic condition (necrotizing fasciitis) and to determine the main predictive factor of health-related quality of life. This study is retrospectively conducted in 18 patients who survived a massive burn injury involving more than 80% of the total body surface area, or more than 70% of the total body surface area if the injury occured during childhood and who were treated between 1997 and 2017 in our Lyon burn center. Short Form-36 Medical Outcomes Survey (SF-36), and Brief Version of Burn Speciļ¬c Health Scale (BSHS-B) are used for the present evaluation.


Description:

The hypotheses are as follows:

- the HR-QOL of massive burns shows a significative alteration compared to general population

- this alteration is comparable with another chronic disease

- the main predictors of impaired quality of life related to physical health status are hand injury, age at time of burn and time since burn

- the main predictive factors of change in quality of life related to mental health status are age of onset and facial involvement.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date August 31, 2018
Est. primary completion date July 31, 2018
Accepts healthy volunteers No
Gender All
Age group 14 Years and older
Eligibility Inclusion Criteria:

1. Patients over 14 years of age

2. Patients with a childhood burn reaching more than 70% of the total body surface OR Adult patients with burns of more than 80% of total body surface area

3. Patients who were treated at the burn center between January 1997 and January 2017

4. Patients who survived after initial hospitalization for burn management

Exclusion Criteria:

1. Patients with superficial burning, without sequelae or with extensive sequelae at less than 70% of total body surface area in children and less than 80% of total body surface area in adults

2. Patients who expressed opposition to their participation in the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Evaluation of health-related quality of life
Short Form-36 Medical Outcomes Survey (SF-36), and Brief Version of Burn Speci?c Health Scale (BSHS-B) are used for the present evaluation.

Locations

Country Name City State
France Hospices Civils de Lyon, Croix-Rousse Hospital Lyon

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Short Form-36 Medical Outcomes Survey (SF-36) sub domain score The impact of massive burn injury is measured for each SF 36 sub domain and compared to general population score. Data concerning HR-QOL was retrospectively collected in July 2018 for all patients with a massive burn injury occuring during 1997 and 2017