None listed
Conditions
Interventions
Intervention1: Dry socket was treated by placing Alveogyl (Manufactured by Septodont India Pvt. Limited) (Content: iodoform 15.8 g, eugenol B.P. 13.7 g, and butamben 25.7 g): To prospectively evaluate
Sponsors
Dr Veeramuthu
Eligibility
Inclusion criteria
Inclusion criteria: Adults of both sexes over the age of 18 who had their teeth extracted and were clinically diagnosed with dry socket. The study included sockets with visible bone, a partial or complete loss of the blood clot at the tooth extraction site, and discomfort radiating from the socket to the same side of the face as the extraction.
Exclusion criteria
Exclusion criteria: Patients over the age of 70 and under the age of 18. A patient with one or more bone disorders, such as osteoporosis. People who have previously taken bisphosphonates orally or intravenously. People who have previously received radiation to the head, neck, or jawbone [9]. Following tooth extraction, patients who reported with pain were examined to identify the cause of their complaint. On the basis of the following characteristics, the clinical diagnosis of dry socket was made. Pain that worsens between one and three days after extraction, in and around the extraction socket, with or without radiation. Alveolar clot loss, whether partial or complete, with or without halitosis.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluating pain score in dry socket treated with AlveogylTimepoint: at day 1, day 4, day 7 | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluating pain score in dry socket treated with warm saline Comparision of pain scores in patients treated with Alveogyl & warm salineTimepoint: At day 1, day 4, day 7 | — |
Countries
India
Contacts
Public ContactVeeramuthu M
Karpaga Vinayaga Institute of dental sciences
Outcome results
None listed