Clinical Trials Directory

Trials / Completed

CompletedNCT01952652

Naproxen Codeine in Arthroscopic Surgery

Comparison of Post-operative Analgesic Effects of Naproxen Sodium and Naproxen Sodium-codeine Phosphate Administered Preemptively for Arthroscopic Meniscus Surgery

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
61 (actual)
Sponsor
Baskent University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

In this study, the aim is to compare the efficacy of single dose naproxen sodium and combination of naproxen sodium-codeine phosphate on post-operative pain in adult patients undergoing arthroscopic menisectomy.Pre-emptive oral naproxen-codeine may be safely and more advantageous than naproxen alone.

Detailed description

Patients receiving preemptive oral naproxen sodium (Group N) or naproxen sodium-codeine phosphate (Group NC) were assigned in 2 groups.Preoperatively, drugs were given orally by a nurse unaware of the study to both groups within 60 minutes before surgery. Hemodynamic datas, possible side effects, pain and sedation levels of patients were recorded. Patient's pain and sedation levels were statistically assessed.

Conditions

Interventions

TypeNameDescription
DRUGGroup N:Naproxen sodiumdrug will be given 60 minutes before surgery
DRUGGroup NC :naproxen sodium codeine phosphatedrug will be given 60 minutes before surgery

Timeline

Start date
2013-01-01
Primary completion
2013-06-01
Completion
2013-07-01
First posted
2013-09-30
Last updated
2013-09-30

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT01952652. Inclusion in this directory is not an endorsement.

Naproxen Codeine in Arthroscopic Surgery (NCT01952652) · Clinical Trials Directory