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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04124822
Other study ID # Dikiohs2013
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date May 30, 2018
Est. completion date July 15, 2019

Study information

Verified date October 2019
Source Dow University of Health Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Two drugs (Piroxicam and Prednisolone)are being compared for post operative endodontic pain after a single visit root canal treatment for 74 hours.


Description:

To evaluate effectiveness of single dose premedication with piroxicam(20mg) and prednisolone(20mg) on post endodontic pain after a single visit root canal treatment .

patient will be recalled every day for 4 days to know the pain scale using visual analogue scale .


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date July 15, 2019
Est. primary completion date July 15, 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

1. Patient ages from 20-40 years(28).

2. Single rooted tooth with symptomatic irreversible pulpitis.

3. With no analgesic or anti-inflammatory drug taken within a week period before procedure.

Exclusion Criteria:

1. Patients presenting with any systemic disease

2. Patients already taking premedication for endodontic pain.

3. Pregnant or lactating patients.

4. Multirooted teeth.

5. Teeth with Pulpal necrosis.

6. Previously treated or initiated root canal treatment.

7. Patient presenting with allergy due to drug

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Piroxicam 20 mg
Piroxicm is from oxicam family of anti inflammatory drug that inhibits prostaglandin synthesis and effectively lower pain threshold levels
prednisolone 20 mg
prednisolone is from steroid family of anti inflammatory drug that inhibit arachidonic acid and effectively lowers the pain

Locations

Country Name City State
Pakistan DUHS Karachi Sindh

Sponsors (1)

Lead Sponsor Collaborator
Dow University of Health Sciences

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary post operative pain post operative pain will be measured after single visit endodontic treatment using visual analog scale with readings 1 to 10 from 24 hours till 76 hours 76 hours