About this trial
The aim of this clinical study will investigate the efficacy of sphenopalatine ganglion block in the treatment of postoperative pain.it will also be learnt whether it reduces the consumption of analgesics in postoperative pain.The main questions it aims to answer are:
Will the participants' need for painkillers decrease after the operation? Can sphenopalatine ganglion block be used for postoperative pain after septoplasty? The researchers will compare 2 groups with and without sphenopalatine ganglion block to see the effectiveness of sphenopalatine ganglion block.
Participants will:
Read the information Participants have been given about the sphenopalatine ganglion block.
In case of any side effects, please contact participant's doctor.
Eligibility criteria
Qualifiers
Participants who will undergo septoplasty
18 to 50 years old
ASA score 1 or 2
Disqualifiers
Under 18 or over 50 years of age
ASA score III and above patient group
The patient is allergic to any of the drugs used
The patient has a contraindication to any of the drugs used
Trial design
Treatments tested in this trial
- Sphenopalatine Ganglion Block