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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04622488
Other study ID # ENDO 3-7-2
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date November 2020
Est. completion date September 2022

Study information

Verified date October 2020
Source Cairo University
Contact Heba El Far, Professor
Phone +201282006589
Email hebaelfar@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to clinically compare the post-operative pain level and antibacterial effect when using the Diclofenac Potassium Insitu gel versus calcium hydroxide as an intra- canal medication in patients with apical periodontitis.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 44
Est. completion date September 2022
Est. primary completion date July 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Age between 18-45 years old. - Males/Females. - Lower permanent premolars with: Non-Vital pulps. Sensitive to percussion. Negative response to cold pulp tester (ethyl chloride spray1). Apical periodontitis - Systemically healthy patients (ASA I or II). Exclusion Criteria: - Medically compromised patients having significant systemic disorders. (ASA III or IV). - History of intolerance to NSAIDS. - Patients with two or more adjacent teeth requiring endodontic treatment. - Teeth with : - Association with swelling or fistulous tract. - Acute or chronic peri-apical abscess. Mobility Grade II or III. - Pocket depth more than 5mm. - Previous root canal therapy. - Non-restorability - Patients with a contraindication for the use of DFK or those known to be allergic to any of the study medications.eg. Patient with kidney problems.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Diclofenac Potassium
- In the form of Insitu gel system can be applied as solution or suspension that undergoes gelation after administration. Applied once inside the root canal after chemo-mechanical preparation.

Locations

Country Name City State
Egypt Faculty of Dentistry Cairo University Cairo El- Manial

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of Post operative pain assessed by VAS Post-operative pain following chemo-mechanical endodontic treatment will be measured.
A pain chart using visual analogue scale (VAS) will be used to record the patients' pain levels. The VAS (0-10 scale) consists of a line anchored by two extremes "No pain" and "the worst pain". Patients will be asked to choose the mark that represented their level of pain from 0 to 10. Pain level will be assigned as follow:
0, "no pain"
1-3, "mild pain"
4-6, "moderate pain"
7-10, "severe pain" Using the VAS chart, the patient will choose and record the most appropriate pain rating according to the pain intensity endured.
72 hours
Secondary Antibacterial effectiveness by measuring the bacterial count. The bacterial count method will be used. Once the samples will arrive to the microbiology department, Cairo University, the tubes containing the thioglycolate 14(transport medium) with the paper points will be placed in micro centrifuge and vortexed for 30 sec. One hundred (100) µl aliquots of the vortexed samples will be placed in a new sterile tube containing 1 ml of thioglycolate to obtain 1/10 concentration to assess the microbial load of common aerobes and anaerobes found in each root canal. The effect of the treatment in each group, the initial colonizers (S1), the mechanical preparation (S2) and after the intra-canal medication (S3) will be compared. pre-operatively(S1), after chemo-mechanical preparation(S2), and after 1 week(S3).
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