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Evaluation of Dental Emergency Treatments During COVID19 Crisis (URGDENTCOVID)

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ClinicalTrials.gov Identifier: NCT04354272
Recruitment Status : Not yet recruiting
First Posted : April 21, 2020
Last Update Posted : April 21, 2020
Sponsor:
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris

Brief Summary:

"For 12 years, the odontology service of the Pitié-Salpêtrière hospital group (GHPS) has been responsible for day and night dental emergency care. Several surveys have been conducted in order to analyze the sociological characteristics of the patients and the typology of the acts performed. These studies indicate that pain is the main reason for consultations, cited by 60 to 80% of patients.

So far, very few studies have been done in the context of emergencies. Very recently, a study was undertaken on the satisfaction of patients consulting the odontological emergencies of the GHPS, during a thesis work.

This study, carried out in collaboration with the URC Pitié Salpêtrière, under analysis, relates to the satisfaction of patients consulting the odontological emergencies of the GHPS during the day and week, Monday to Friday, excluding night and week emergencies -end (WE). An additional study (URGDENT-NW) aiming at completing this study by focusing on patients consulting the emergency room at night and during the weekend is also in progress.

The COVID19 Crisis changed the organization and the venue of patients at the emergency dental service.

Therefore this project, based on the same protocol as URGENT and URGDENT-WE, aims at evaluating the Odontology Emergency Reception Service (SAUO) during the COVID 19 epidemy. It will be carried out in the form of a survey whose objective is to assess: on the one hand, the effectiveness of the care provided in this emergency functional unit, and on the other hand the satisfaction of the patients after their passage to the emergency room ."


Condition or disease Intervention/treatment
Orofacial Pain Orofacial Edema Dental Trauma Oral Infection Other: Questionnaire

Show Show detailed description

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Study Type : Observational
Estimated Enrollment : 840 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Evaluation of the Management of Dental Emergencies During COVID 19 Crisis
Estimated Study Start Date : April 13, 2020
Estimated Primary Completion Date : June 20, 2020
Estimated Study Completion Date : June 20, 2020

Group/Cohort Intervention/treatment
Questionnaire Other: Questionnaire
Questionnaire for the satisfaction of patients consulting the odontological emergencies of the GHPS during COVID 19.




Primary Outcome Measures :
  1. Pain score evolution measured by a 0-10 numeric scale (NS) where 0 is no pain and 10 the worst pain imaginable [ Time Frame: Day 1 ]
    "Self report measure of pain on the numeric scale 24h after the visit "


Secondary Outcome Measures :
  1. Pain scores evolution 3 days and 7 days after first visit measured by a numeric scale where 0 is no pain and 10 the worst pain imaginable [ Time Frame: Day 3 and Day 7 ]
    the pain is measured with the numeric scale

  2. welcoming quality from hospital staff [ Time Frame: Day 1 ]
    Perception of welcoming, waiting time will be measured with a 0-10 numeric scale

  3. anxiety score [ Time Frame: Day 0, Day 1, Day 3, Day 7 ]
    The patient anxiety will be measured by numeric scale at Day 0, Day 1, Day 3, Day 7

  4. perception of the technical quality of the emergency treatment [ Time Frame: Day 1 ]
    The perception is measured just after care with a 0-10 numeric scale



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
patients seeking care at the dental emergency serviceduring COVID 198 crisis
Criteria

Inclusion Criteria:

  • Age ≥ 18 years
  • Patient reachable by telephone during the week following his / her care in the service
  • Collection of the consent of the patient for his participation in research
  • Good understanding of the French language

Exclusion Criteria:

-Patient with communication difficulties or difficulties in understanding the French language"


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04354272


Contacts
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Contact: Yves Boucher, MD, PhD 01 42 16 14 51 yves.boucher@aphp.fr
Contact: Isabelle Rodriguez iba.rodriguez@gmail.com

Sponsors and Collaborators
Assistance Publique - Hôpitaux de Paris
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Responsible Party: Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier: NCT04354272    
Other Study ID Numbers: APHP200464
First Posted: April 21, 2020    Key Record Dates
Last Update Posted: April 21, 2020
Last Verified: April 2020

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Emergencies
Facial Pain
Disease Attributes
Pathologic Processes
Pain
Neurologic Manifestations