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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05478044
Other study ID # ENDO 3 - 7 - 1
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 2022
Est. completion date August 2023

Study information

Verified date July 2022
Source Cairo University
Contact Kariman Amin Ismaiel, B.D.S faculty of dentistry
Phone +20 1013665586
Email kariman.ameen@dentistry.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is conducted to evaluate the effect of Ascorbic acid as a final flush on post operative pain after single visit root canal treatment in cases with symptomatic irreversible pulpits.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date August 2023
Est. primary completion date August 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Patients above 18 years old and to 60. - Male or female. - Patients seeking root canal treatment. - mandibular molar teeth with symptomatic irreversible pulpits with preoperative acute or moderate pain with hot and cold stimulation with normal periapical radiographic appearance . - healthy patient (ASA I,II). - Patient who can understand NRS and sign informed consent. Exclusion Criteria: - Medically compromised patients having significant systemic disorders. (ASA III or IV). - History of intolerance to NSAIDS. - External root resorption. - Internal root resorption. - Vertical root fracture. - Periapical lesion. - Pregnancy. - Use of ibuprofen in the last 12 hour. - Bleeding disorder. - Long term corticosteroid use. - Mobility Grade II or III. - Pocket depth more than 5mm. - Previous root canal therapy. - Non-restorability. - TMJ problems, bruxism, clenching or traumatic occlusion. - Inability to perceive the given instructions.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ascorbic acid
Ascorbic acid IV ampoules (20%).
Other:
saline
saline (0.9%)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary Pain intensity measured by numerical rating scale where 0= no pain, 1-3= mild pain, 4-6= moderate pain and 7-10= severe pain. up to 48 hours after root canal treatment.
Secondary If there are analgesics taken by the patient after root canal treatment and that will be measured by a questionnaire. up to 48 hours.
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