Analgesia, Healing Wound, Hemorrhage, Pain, Postoperative
Conditions
Brief summary
In our study, three different medicaments were evaluated in terms of postoperative complications after free gingival grafting (FGG).
Detailed description
In our study, three different medicaments were evaluated in terms of postoperative complications after free gingival grafting. The effectiveness of these 3 different commercially available agents containing flurbiprofen, hyaluronic acid, and hypochlorous acid, after use 2., 4.7. and on the 14th day, wound healing and pain perception was compared with the control group. primary observation was obtained by visual analog scale, wound healing index, bleeding of tissue, color match, and amount of painkiller used by the patient were also recorded
Interventions
DRUGMajezik %0.25 oral spray
Free gingival graft was taken from the palatal mucosa of the patients in order to increase the attached gingiva. After FGG, the patients were asked to apply this spray to the palatal mucosa 3 times a day.
OTHERAftamed oral spray
Free gingival graft was taken from the palatal mucosa of the patients in order to increase the attached gingiva. After FGG, the patients were asked to apply this spray to the palatal mucosa 3 times a day.
OTHERCrystalin oral spray
Free gingival graft was taken from the palatal mucosa of the patients in order to increase the attached gingiva. After FGG, the patients were asked to apply this spray to the palatal mucosa 3 times a day.
PROCEDUREFree gingival graft harvesting
Free gingival graft was taken from the palatal mucosa of the patients in order to increase the attached gingiva.
Sponsors
Pamukkale University
Study design
Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
- Patients with systematic conditions are classified as The American Society of Anesthesiologists Class I \-
Exclusion criteria
* Pregnancy, lactation, and taking contraceptive pills. * Oversensitivity or anaphylactic reactions which contraindicate the intervention. * Orofacial neurological symptoms. * Infections at operation zone. * Psychotropic medicine, sedative, or non-steroid anti-inflammatory drugs use which can alter the sense of pain. * Pathological mental conditions (dementia, psychosis) and lack of cooperation. * Smoking * Excessive gag reflex * Operations are carried out with conscious sedation. * Patients who do not want to sign consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Landry's Wound Healing Index (WHI) | 21 days | WHI was performed on the basis of postoperative healing characteristics categorized as tissue color, response to palpation, incision margins, and suppuration. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Visual Analogue Scale | 21 days | Recording the pain perception of the patients on a scale from 0 to 10. 0 - no pain 10 - worst pain |
| Color match | 21 days | scoring the color match of the healed tissue area with the patient's remaining tissue |
| delayed bleeding | 21 days | examining the patient whether there is postoperative bleeding, if there is a positive, if not, it should be recorded as negative. |
| burning sensation | 21 days | Evaluation of the burning sensation felt in the healing area of the patient's palate from 0 to 10. 0-no burning sensation 10- excessive burning |
| complete epithelization | 21 days | Examination of epithelialization with 3% oxygenated water. keeping records according to the foaming rate in the tissue |
Countries
Turkey (Türkiye)
Outcome results
None listed