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Pre-hospital Care Profile of Road Traffic Injury Victims- Kerala (PCP-K)

9 februari 2021 uppdaterad av: Dr. Sr. Alphonsa Mathew, Jubilee Mission Medical College and Research Institute

Pre-hospital Care Profile of Road Traffic Injury Victims Presenting to the Emergency Department of a Tertiary Care Centre in Kerala, a Cross-sectional Study

Selection of appropriate strategies and correct policy-making in these conditions may lead to decreased rates of death due to RTI.There is a lack of research on the effectiveness of pre-hospital care in Kerala. This study aimed to describe the prehospital care of RTI victims presenting to the emergency department in Jubilee Mission Medical College and Research Institute, Thrissur.

Studieöversikt

Status

Avslutad

Betingelser

Intervention / Behandling

Detaljerad beskrivning

Management of trauma is a neglected field in developing nations.Road Traffic Injuries (RTI) cause around 1.35 million deaths worldwide annually according to the statistics of World Health Organization (WHO) and in India 150000 death per year. An overwhelming proportion of these deaths occur before patients even reach the hospital. Two third (60.7%) of the accident victims belonged to the age range of 15 to 44 years. This indicates that active and productive age people are the one affected by road traffic accidents related injuries in turn adding to higher economic loss to the country. Lack of medical attention is attributed to nearly 30 per cent of deaths at site and 80 per cent of the remaining patients died within an hour of injury (golden hour). Most of these deaths are due to airway management failure, respiratory failure or continuing hemorrhage that are preventable causes with appropriate prehospital and subsequent hospital emergency care. Mortality due to RTI is increasing, especially in Low and Middle Income Countries (LMIC). There is a lack of research on the effectiveness of pre-hospital care in India. Selection of appropriate strategies and correct policy-making in these conditions may lead to decreased rates of death due to RTI in several countries.This study aimed to describe the prehospital care of RTI victims presenting to the emergency department (ED) in Jubilee Mission Medical College and Research Institute, Thrissur.

Studietyp

Observationell

Inskrivning (Faktisk)

978

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

  • Indien
    • Kerala
      • Thrissur, Kerala, Indien, 680005
        • Jubilee Mission Medical College and Research Institute

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn
  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Testmetod

Icke-sannolikhetsprov

Studera befolkning

All RTI patients presenting to ED within 24 hours of injury irrespective of gender, race or comorbidities involved in an RTI would be approached to be recruited for the study.

Beskrivning

Inclusion criteria:

All Road traffic injury (RTI) patients presenting to ED within 24 hours of injury

Exclusion criteria:

Individual's not consenting to be part of the study or withdrawing consent later on

Cases where pre-hospital care provider could not be traced or where reliable patient data could not be collected even after repeated interview.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Kohorter och interventioner

Grupp / Kohort
Intervention / Behandling
Road traffic injury victims

All RTI patients presenting to ED within 24 hours of injury is included in the study..

Individual's not consenting to be part of the study or withdrawing consent later on would be excluded. We also would exclude cases where pre-hospital care provider could not be traced or where reliable data patient could not be collected even after repeated interview.
Övrig: Interview

Trained research assistants would abstract the data as per a preset proforma. The data would be collected from the patient (if coherent), pre-hospital care provider or primary care provider.

Data would was also obtained from patient records and the proforma filled by the attending doctors on duty.

Follow up of cases would be done until discharge from the hospital.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Pre-hospital care profile of RTI Victims presenting to the emergency department in a tertiary care center in Kerala as measured by a questionnaire.
Tidsram: Hospital admission days through discharge; up to 30 days
Pre-hospital care received by RTI Victims presenting to the emergency department in a tertiary care center in Kerala
Hospital admission days through discharge; up to 30 days

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Jubilee Mission Medical College and Research Institute

Utredare

  • Studiestol: Salish Varghese, MD, salishvarghese@gmail.com

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

1 januari 2019

Primärt slutförande (Faktisk)

30 april 2019

Avslutad studie (Faktisk)

31 juli 2019

Studieregistreringsdatum

Först inskickad

29 september 2020

Först inskickad som uppfyllde QC-kriterierna

4 oktober 2020

Första postat (Faktisk)

8 oktober 2020

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

11 februari 2021

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

9 februari 2021

Senast verifierad

1 februari 2021

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • 36/18/IEC/JMMC&RI
  • CTRI/2019/03/018160 (Annan identifierare: Clinical trial registry India)

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

JA

IPD-planbeskrivning

Individual participant data would be shared once published in a peer reviewed journal.

Tidsram för IPD-delning

from 2025 for a period of 1 year

IPD-delning som stöder informationstyp

  • STUDY_PROTOCOL
  • ICF
  • CSR

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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