impacted third molar. Embedded and impacted teeth
Conditions
Interventions
Intervention 1: intervention: after surgical removal of tooth ,the socket was chosen randomized and it was filled with OCHS (OSTEORA® 0.5 ml) until it got overfilled. Intervention 2: control:after sur
Prevention
intervention: after surgical removal of tooth ,the socket was chosen randomized and it was filled with OCHS (OSTEORA® 0.5 ml) until it got overfilled
control:after surgical removal of impacted third molar On the other side we just pretended to put it in the socket (control group) and the patient was convinced that we had put the material on the bot
Sponsors
Reserch Center of Tehran azad university of medical sciences
Eligibility
Sex/Gender
All
Age
17 Years to 40 Years
Inclusion criteria
Inclusion criteria: All patients whom underwent this surgery were between 17-40 years old that had the indication for exacting wisdom tooth surgery; had bilateral teeth (maxilla or mandible) and these teeth had the same criteria as in four point trauma rating scale and Pederson. Patients consciously agreed to cooperate with this study and promising incorporation. patients will be excluded if: having acute or chronic pericoronitis; using drugs except the drugs which were considered in the study; their disinclination for evaluation; not filling out or handing the forms; having systemic problems; pregnancy; considered drug prohibition for the patient; having allergic history to the considered drug; having painful conditions in the mouth like having teeth with root canal therapy indication; having any algogenic condition in the body; having nervous system diseases; having a need for prophylaxis; patients using steroids, antidepressant, antibiotics, analgesics; having complications during surgery; inferior alveolar canal exposure; applying more traumatic pressure in one side; having the condition that four bony walls were not available for putting the material; condition were having same numbers of sutures were not possible; disability in suturing the flap completely.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: immediate,1,6,12,24,32,48,72 hours after surgery. Method of measurement: The amount of pain depending on VAS of pain.;Healing. Timepoint: immadiate,3 and 7 days after surgery. Method of measurement: with healing scale.;Dry socket. Timepoint: 3-4 days after surgery. Method of measurement: inspection of signs and symptoms.;Infection. Timepoint: 3-7 days after surgery. Method of measurement: inspection of signs and symptoms.;Bleeding. Timepoint: immediate,8-24 hours , 24-72 hours after surgery. Method of measurement: inspection of signs and symptoms. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactdr. saifollah hemmat
tehran azad university of medical sciences, dental faculty
Outcome results
None listed