Actively Recruiting
Single Dose Preemptive Paracetamol or Ibuprofen Before Septrorhinoplasty on Intra- and Postoperative Opioid Consumption.
Led by Samsun University · Updated on 2026-01-13
54
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Reducing intra- and postoperative pain or using less opioids is an essential strategy in today's operations. One emerging and widely used method in this context is the use of preemptive analgesic medication. Paracetamol and ibuprofen used preemptively have been shown to reduce postoperative opioid use and pain scores. There are also studies showing that preemptive analgesia with different analgesic medications reduces opioid consumption and postoperative pain. Our study will evaluate both the intraoperative and postoperative effectiveness of paracetamol and ibupurofen with preemptive analgesia, considering total opioid use. It will also investigate drug side effects and their advantages using a 15-question compilation quality scale, validated in Turkish.
CONDITIONS
Official Title
Single Dose Preemptive Paracetamol or Ibuprofen Before Septrorhinoplasty on Intra- and Postoperative Opioid Consumption.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Undergoing septorhinoplasty surgery
- ASA physical status 1 or 2
- Men and women aged 18 to 65 years
- Able and willing to provide informed consent and participate in the study
You will not qualify if you...
- ASA physical status 3 or 4
- Under 18 years of age
- Serious kidney, liver, heart, or lung diseases
- Allergy to paracetamol or ibuprofen
- Bleeding disorders, platelet dysfunction, gastrointestinal disease, or peptic ulcer
- Pregnancy, planning pregnancy, or breastfeeding
- Use of aspirin or other anticoagulant medications
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Samsun University Samsun Training and Research Hospital
Samsun, Turkey (Türkiye)
Actively Recruiting
Research Team
H
Hasan Cetinkaya, M.D.
CONTACT
C
Caner Genc, M.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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