A prospective double - blind randomized placebo - controlled clinical trial to evaluate the efficacy of dextrose prolotherapy with and without local anesthetic for temporomandibular joint subluxation / Esam Ahmed Mohammed Obaid ; Supervised Hamida Refai Hassanien , Nadia Jalal
Material type: TextLanguage: English Publication details: Cairo : Esam Ahmed Mohammed Obaid , 2014Description: 62 Leaves : photographs ; 30cmOther title:- دراسة سريرية عشوائية محجوبة الإزدواجية لتقييم فعالية المعالجة المكثرة باندكستروز مع و بدون انمخدر الموضعى على خلع انًفصل انفكى انصدغى [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Date due | Barcode | |
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Thesis | قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.09.13.M.Sc.2014.Es.P (Browse shelf(Opens below)) | Not for loan | 01010110065474000 | |||
CD - Rom | مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.09.13.M.Sc.2014.Es.P (Browse shelf(Opens below)) | 65474.CD | Not for loan | 01020110065474000 |
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Thesis (M.Sc.) - Cairo University - Faculty of Oral and Dental Medicine - Department of Oral and Maxillofacial Surgery
The aim of the this study was to determine if mixing dextrose with local anesthetic could alter the clinical outcome of dextrose prolotherapy for TMJ subluxation. Eighteen patients with painful subluxation of the TMJ were randomly assigned to 1 of 2 equal - sized groups. Patients in the active group received 4 injections of dextrose solution (2 mL of 10% dextrose and 1 mL of 2% mepivacaine) for each TMJ, each 6 weeks apart, whereas patients in the placebo group received injections of placebo solution (2 mL of 10% dextrose and 1 mL of saline solution) on the same schedule. A numerical rating scale (NRS) expressing TMJ pain on rest and during function, maximal mouth opening (MMO), clicking sound, and frequency of luxations (number of locking episodes per month) were assessed at each injection appointment just before the injection procedure and 3 months after the last injection. The collected data were then statistically analyzed. All the evaluated parameters showed insignificant differences between the two groups throughout the study intervals with the exception that pain on function at 18 weeks postoperatively significantly decreased in group 1 than in group 2 and the number of analgesic intake was significantly decrease in group 1 compared to those in group 2 at 6 weeks and 3 months after injection
Issued also as CD
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