Ignite Creation Date:
2024-05-06 @ 6:30 PM
Last Modification Date:
2024-10-26 @ 2:49 PM
Study NCT ID:
NCT05681494
Status:
NOT_YET_RECRUITING
Last Update Posted:
2023-02-16
First Post:
2022-12-28
Brief Title:
Assessment of Pain and Treatment Success After VPT Versus RCT in Mature Permanent Mandibular Molars With SIP A RCT
Sponsor:
Cairo University
Organization:
Cairo University
Study Overview
Official Title:
Assessment of Postoperative Pain and Treatment Success After Vital Pulp Therapy Versus Root Canal Treatment in Mature Permanent Mandibular Molars With Irreversible Pulpitis A Randomized Controlled Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2023-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Assessment of postoperative pain and treatment success after vital pulp therapy versus root canal treatment in mandibular molar with signs and symptoms of irreversible pulpitis the null hypothesis there is no difference will be observed in the pain level and treatment success between two treatments
Detailed Description:
After proper clinical and radiographic examination Teeth will be anesthetized and isolated using a rubber dam The operative field will be disinfected Total caries removal will be done from outside making margin caries free to inside the new diamond bur will be used to remove the last layer and exposed the pulp tissue Exposed pulp will be inspected under a dental operating microscope and hemostasis will be obtained The teeth will be randomized into 2 intervention groups VPT or RCT Treatment will be finalized and teeth will be restored with resin-modified glass ionomer followed by composite resin at the same appointment Ibuprofen 400mg will be prescribed to the patient if needed Patients will be asked to record postoperative pain after treatment on the pain score sheet
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None