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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03591172
Other study ID # CEBD_CU_2018_05_29
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2018
Est. completion date September 2019

Study information

Verified date May 2018
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

this study will assess different irrigating materials on the success revascularization of necrotic mature teeth associated with PRF.


Description:

Nano-propolis and Propolis will be used as final endodontic irrigants and will be compared to saline in Revascularization of necrotic mature teeth.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 75
Est. completion date September 2019
Est. primary completion date November 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 40 Years
Eligibility Inclusion Criteria:

- mature teeth.

- teeth with periapical periodontitis.

- Maxillary anterior teeth

- Patients should be free from any systemic disease

- Patients who will agree to the consent and will commit to follow-up period.

Exclusion Criteria:

- Patients with immature roots.

- Patients with any systemic disease that may affect normal healing.

- Patients with swelling. .Pregnant females. .Patients who could/would not participate in a 1-year follow-up. .Patients with fistula. .Patients with old age. .Teeth with periodontal involvement. .Teeth with vertical root fractures. .Non-restorable teeth.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Propolis
Using propolis as a final irrigation in revascularization
Nano-propolis
Using Nano-propolis as a final irrigation in revasculariztion
saline
Using saline as a final irrigation in revasculariztion

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary post-operative pain: Visual analogue scale post-operative pain evaluated using Visual analogue scale , 0 no pain, 10 severe pain. 1 year
Secondary periapical healing evaluated radiographically 1 year
Secondary sensitivity electric pulp tester 1 year
Secondary survival clinical evaluation 1 year
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