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In the blood sample of the patients planned for nasal septoplasty was evaluated the level of opioid analgesic receptor and the relations between the level of receptor and pain score,

The relations between the level of Mu-opioid receptor (µORs) and postoperative analgesic use in patients undergoing septoplasty: a randomized, prospective trial.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619001652167
Enrollment
120
Registered
2019-11-26
Start date
2015-06-05
Completion date
2019-01-24
Last updated
2019-12-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

we aimed to investigate whether there is a relationship between opioid receptor level and postoperative pain intensity 120 adult patients underwent septoplasty were randomly divided into preop 2 groups. The first group (n=60) was patients given tramadol (1-2 mgr/kg) for postop analgesia, and the second group (control group)(n=60) was initially performed only fentanyl (1 µg/ kg-i.v.) in the induction.

Interventions

All patients were randomly selected to have into two groups. For postoperative analgesia, the first group (n=60) is patients using tramadol (1-2 mgr/ kg, intravenously) at the end of the surgery for postoperative analgesia. It is single dose. The second group is control group, and patients are initially given only fentanyl in the induction for analgesia. Fentanyl (1 µg/ kg, intravenously), propofol (2-3 mgr/ kg, intravenously), and muscle relaxant (rocuronium bromide 0,6 mgr/ kg, intravenously)

All patients were randomly selected to have into two groups. For postoperative analgesia, the first group (n=60) is patients using tramadol (1-2 mgr/ kg, intravenously) at the end of the surgery for postoperative analgesia. It is single dose. The second group is control group, and patients are initially given only fentanyl in the induction for analgesia. Fentanyl (1 µg/ kg, intravenously), propofol (2-3 mgr/ kg, intravenously), and muscle relaxant (rocuronium bromide 0,6 mgr/ kg, intravenously) are administered to all patients for induction as single dose. The medications were given intravenously to each group before awakened were performed by the Anesthesia Care Team. All the patients’ vital signs were monitored during the operation. We planned to audit of anesthesia nurse notes to assess or monitor fidelity to the intervention.

Sponsors

MUZAFFER GENCER
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Primary purpose
Diagnosis

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

Patients undergoing septoplasty

Exclusion criteria

Patients with surgical planning except septoplasty

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 26, 2026