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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05568563
Other study ID # Ethyl Chloride versus Honey
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2022
Est. completion date September 30, 2022

Study information

Verified date October 2022
Source Altamash Institute of Dental Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparing Pre-cooling with Ethyl Chloride versus Honey in Alleviating Intra-oral injection pain in Adult patients


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date September 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - No medical history - Patients suffering from Symptomatic Irreversible Pulpitis requiring buccal infiltration Exclusion Criteria: - Patients having any medical conditions considered to affect patient safety or the quality of the study - if they had any known hypersensitivity to local anaesthetics of amide type or any of the other contents in the substance used

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ethyl chloride
Ethyl chloride is an agent that is widely used in dental practice as the standard modality for pulp vitality tests .
Other:
Honey
Honey is a natural dietary product

Locations

Country Name City State
Pakistan Hira Danish Karachi Sindh

Sponsors (1)

Lead Sponsor Collaborator
Altamash Institute of Dental Medicine

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary To alleviate dental injection pain Post administration of oral local anesthetic infiltration pain will be measured by using Visual Analogue Scale(VAS) which is an 10-point scale from 0-10 where 0 represents no pain and 10 represents the worst pain measured immediately after completion of administration of oral local anesthetic infiltration within 60 seconds
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