Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06613932
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-08-16
Brief Title:
Assessment of L-PRF Nanohydroxyapatite Combined With L-PRF Using Pulpotomy in Mature Mandibular First Molars
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Clinical and Radiographic Assessment of L-PRF Nanohydroxyapatite Material Combined With L-PRF Scaffold in Vital Pulp Therapy Treatments in Mandibular First Molars With Closed Apices Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Clinical and Radiographic Assessment of L-PRF Nanohydroxyapatite material combined with L-PRF scaffold in Vital pulp Therapy Treatments in Mandibular First Molars with Closed Apices Randomized Controlled Trial
Detailed Description:
pulpotomy by using 3 materials The first groupcontrol group uses hydroxyapatite material as a pulpotomy agent and the second group uses L-PRF as a pulpotomy agent the third group uses combined material L-PRF Nano hydroxyapatite as a pulpotomy agent then assesses the clinical and radiographic result of the 2 interventions group with control group
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None