Ignite Creation Date:
2024-05-06 @ 1:46 AM
Last Modification Date:
2024-10-26 @ 11:09 AM
Study NCT ID:
NCT01896427
Status:
UNKNOWN
Last Update Posted:
2013-07-11
First Post:
2013-06-30
Brief Title:
Comparing Pain and Swelling After Surgical Extraction of Mandibular Third Molar in Dexamethasone Injection and Without Corticosteroid Methods
Sponsor:
Mohammad Javad Shirani
Organization:
Isfahan University of Medical Sciences
Study Overview
Official Title:
None
Status:
UNKNOWN
Status Verified Date:
2013-07
Last Known Status:
RECRUITING
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:
In some cases impacted wisdom teeth should be extracted Surgical extraction of these impacted third molars may provide special complication as pain swelling and trismus In previous studies some techniques as sutureless flap closure modified flap designing antibiotic usage and injection of corticosteroids were presented These methods are reducing post operative complications to moderate level In this study pain swelling trismus general patients satisfaction and associated quality of life after the surgical removal of third mandibular impacted molars will be compared while injection of dexamethasone 8mg does not need excessive time effort and equipments and it will be injected in numbness area into medial pterygoid muscle and pterygomandibular space to current corticosteroid injecting non-corticosteroid methods To achieve this aim 75 non pregnant participants have single impacted mandibular third molar in healthy and without pericoronitis manner after provision of written informed consent will be entered to the study During the study unwilling participants to continue the study and those with abnormality of wound healing process will be excluded The included participants will be assigned into three 25-people groups The surgeries were done by 3 same instructed experienced oral and maxillofacial residents After the surgery pain swelling trismus general patients satisfaction and associated quality of life were evaluated using interview of questionnaire in 48 hour 96 hour and one week period of time The comparison was done between these three groups
Detailed Description:
None
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
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 292037 | OTHER_GRANT | None | None |
| IRCT2013042713140N1 | REGISTRY | Iranian Registry of clinical trials | None |