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The Effect of Bilateral Sphenopalatine Ganglion Block on Postoperative Pain in Patients to be Subject to Septorhinoplasty Surgery

S

Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital

Status

Completed

Conditions

Anesthesia of Mucous Membrane

Treatments

Procedure: placebo
Procedure: Bilateral endoscopic sphenopalatine ganglion block

Study type

Interventional

Funder types

Other

Identifiers

NCT06016816
HTosunSoner

Details and patient eligibility

About

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.

Enrollment

72 patients

Sex

All

Ages

17 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

72 participants in 2 patient groups, including a placebo group

Endoscopic bilateral sphenopalatine ganglion block
Active Comparator group
Description:
After the induction of general anesthesia, one group (Group: 1) will be administered 8mg dexamethasone and 10mg bupivacaine submucosal,
Treatment:
Procedure: Bilateral endoscopic sphenopalatine ganglion block
Placebo
Placebo Comparator group
Description:
Placebo group (group:2) will be administered 4 cc saline. aspects will be evaluated.
Treatment:
Procedure: placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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