Postoperative Pain After Pulpectomy of Primary Molars Using Two Different Root Canal Obturation Techniques: A Randomized Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Testing postopertive pain after pulpectomy of primary molars with endoflas using modified Wong-Baker scale of pain.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 5
Maximum Age: 7
Healthy Volunteers: f
View:

• The current study will include children who meet the following clinical and radiographic criteria:

• 1a.Clinical:

⁃ 5-7-year old children categorized as class I or II according to American Society of Anaesthesiologists (ASA) scale.

⁃ Children rated as no.3 or 4 in Frankel behavior rating scale (FBRS).

⁃ Presence of at least one primary molar with deep carious lesion.

⁃ Asymptomatic necrotic molars confirmed by the absence of bleeding on opening of the pulp chamber.

• 1b. Radiographic:

⁃ Extensive caries approaching to the pulp.

⁃ Presence of at least two-thirds of root length.

Locations
Other Locations
Egypt
Shimaa Mohamed Abd Elhafeez
RECRUITING
Minya
Contact Information
Primary
shimaa m abd elhafeez, postgraduate
drshimaaalhhafeez93@gmail.com
+0201068976757
Backup
Osama s Gad El-Hak, phD
osama.seif@mu.edu.eg
00201023449797
Time Frame
Start Date: 2024-01-20
Estimated Completion Date: 2024-06
Participants
Target number of participants: 100
Treatments
Experimental: lentilospiral group
Obturation of primary molars with calcium hydroxide, eugenol and iodoform paste using paste carrier files(lentiospiral files)
Active_comparator: pressure seringe group
Obturation of primary molars with calcium hydroxide, eugenol and iodoform paste using pressure seringe
Related Therapeutic Areas
Sponsors
Leads: Minia University

This content was sourced from clinicaltrials.gov