Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06631885
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-13
Brief Title:
Efficacy of Integrated Nano-technology in Revascularization of Immature Necrotic Teeth
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Efficacy of Integrated Nano-technology in the Irrigation Protocol of Revascularization Technique In Immature Necrotic Teeth Randomized Clinical Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
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:
This trial aims to study the effect of photoactivated disinfection using Diod laser 810 nm to activate photosensitive nanoparticle chitosan as an endodontic irrigant versus sodium hypochlorite followed by saline and then EDTA 17 on 1 postoperative pain and 2 the success of revascularization in patients with necrotic immature maxillary anterior teeth using a randomized clinical trial design
Detailed Description:
randomized clinical trial will be conducted to investigate and compare the efficacy of photosensitized nano-chitosan 2 as an endodontic disinfectant during revascularization versus sodium hypochlorite followed by EDTA 17 according to the standardized protocol of the American Association of endodontics
Twenty individuals with necrotic immature permanent anterior teeth will be recruited They will be randomly assigned into two groups according to the received intervention control group and test group
pain will be evaluated as a primary outcome at 24 hours and one week post-intervention using numerical rating scale NRS In addition the root development in terms of change in root length and apical foramen diameter and periapical bone healing will be evaluated as secondary outcomes using cone beam tomography
Twenty individuals with necrotic immature permanent anterior teeth will be recruited They will be randomly assigned into two groups according to the received intervention control group and test group
pain will be evaluated as a primary outcome at 24 hours and one week post-intervention using numerical rating scale NRS In addition the root development in terms of change in root length and apical foramen diameter and periapical bone healing will be evaluated as secondary outcomes using cone beam tomography
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