The Effect of Bilateral Sphenopalatine Ganglion Block on Postoperative Pain in Patients to be Subject to Septorhinoplasty Surgery
- Conditions
- Anesthesia of Mucous Membrane
- Interventions
- Procedure: Bilateral endoscopic sphenopalatine ganglion blockProcedure: placebo
- Registration Number
- NCT06016816
- Lead Sponsor
- Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
- Brief Summary
The aim of this study is to examine the effects of bilateral sphenopalatine ganglion block on surgical conditions, hemodynamics, intraoperative and postoperative analgesic use, recovery characteristics, and postoperative pain during septorhinoplasty under general anesthesia. The study was planned as double-blind, randomized, controlled. 72 patients who will undergo septorhinoplasty surgery will be collected. (g power analysis was performed.) Evaluation of the effectiveness of bilateral sphenopalatine ganglion block was planned. Patients will be divided into 2 equal groups (36 patients). After the induction of general anesthesia, one group (Group: 1) will be administered 8mg dexamethasone and 10mg bupivacaine submucosal, the other group (group:2) will be administered 4 cc saline. aspects will be evaluated.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 72
- patients with an ASA score of I-II and between the ages of 17-45 years, who were to undergo general anesthesia with desflurane, were included in the study.
- Patients aged <17 and >45 years, patients with liver and/or kidney failure, obese patients (BMI >30), trauma patients, ASA III-IV patients, patients with bleeding disorders, those using drugs that may affect the coagulation system, patients with cardiomyopathy, cerebrovascular disease, immobility, and malnutrition were excluded from the study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Endoscopic bilateral sphenopalatine ganglion block Bilateral endoscopic sphenopalatine ganglion block After the induction of general anesthesia, one group (Group: 1) will be administered 8mg dexamethasone and 10mg bupivacaine submucosal, Placebo placebo Placebo group (group:2) will be administered 4 cc saline. aspects will be evaluated.
- Primary Outcome Measures
Name Time Method Numeric Rating Scale Postoperative 0-2 hours, 2-8 hours,8-24 hours They will be numbered from 1 to 10.
1 mildest 10 most severe pain
- Secondary Outcome Measures
Name Time Method intraoperative remifentanil consumption intraoperative The intraoperative ultiva infusion dose was recorded to the patient.
Riker Agitation Scale Immediately after extubation 7 Dangerous Agitation 6 Very Agitated 5 Agitated 4 Calm and Cooperative 3 sedated 2 Very Sedated A
1 Unarousableedema questionnaire Postoperative 0-2 hours, 2-8 hours,8-24 hours Periorbital edema was evaluated as present or absent questionnaire
mean arterial pressure when you come to the operating room table after anesthesia induction Intraoperative 30 minutes after extubation mmhg
hematoma questionnaire Postoperative 0-2 hours, 2-8 hours,8-24 hours Hematoma was evaluated as present or absent questionnaire
heart rate when you come to the operating room table after anesthesia induction Intraoperative 30 minutes after extubation beats\\minute
vomiting questionnaire Postoperative 0-2 hours, 2-8 hours,8-24 hours was evaluated as present or absent questionnaire
Oral analgesic use In the first 24 hours after surgery Analgesic use in the first 24 hours was questioned.
Trial Locations
- Locations (1)
Health Sciences University Gazi Yaşargil Training and Research Hospital
🇹🇷Diyarbakır, Kayapınar, Turkey