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Effect of NLR and MPV on Early Postoperative Outcome in Lower Extremity Arthroplasty Operations

Effect of Neutrophil /Lymphocyte Ratio (NLR) and Mean Platelet Volume (MPV) on Early Postoperative Outcome in Lower Extremity Arthroplasty Operations

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03148951
Enrollment
754
Registered
2017-05-11
Start date
2017-06-28
Completion date
2018-01-31
Last updated
2023-01-13

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

Conditions

Knee Arthropathy

Keywords

MPV, NLR, Postoperative pain

Brief summary

In the planned study the investigators want to evaluate the relation between postoperative complications and minor/ major morbidities, mortality and Mean Platelet Volume (MPV) and Neutrophil/ lymphocyte (N/L) ratio.

Detailed description

* In this study the investigators aim to determine the relation between the MPV and N/L ratio and the incidence of postoperative adverse events and complications in patients undergoing knee arthroplasty. * In this study only the laboratory tests that are routinely used for the operative patients are going to be used and no extra tests will be performed. The study will begin after the postoperative blood samples are collected for routine laboratory measurements. The patients will be allocated to 4 groups according to the type of anesthesia and VAS scores. Preoperative and postoperative peripheral blood total whole blood MPV and N/L ratio and 1st 6th 12th ve 24th hours VAS scores and complications, morbidities and mortality will be recorded. The patients will receive analgesics according to the routine practice in the ward and the doses of analgesics given will be recorded at 1st 6th 12th ve 24the hours wil be recorded. * Statistical analysis: the numerical variables will be analyzed tested with Kolmogorov-Smirnov test for normality. For the parametric variables that are normally distributed t-test will be used for the comparison between groups. For the parametric variables that are not normally distributed Mann Whitney-U test will be used. All the categorical variables will be evaluated with q- square tests. A p value \< 0.05 will be determined as statistically significant.

Interventions

None listed

Sponsors

Akdeniz University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* knee arthroplasty patients with general or spinal anesthesia.

Exclusion criteria

* patients not giving consent * reoperations * patients having inflammatory disease * infection in the knee * sepsis * bleeding disorders * hematologic diseases, * using steroids. * trauma * fracture patients, * bilateral knee prothesis * combined surgery procedures * patients needing perioperative transfusions * uncooperative patients.

Design outcomes

Primary

MeasureTime frameDescription
postoperative VAS (visual analogue scale) scoreVAS score at postoperative twenty-forth hours will be evaluatedpostoperative visual analog scale score for pain evaluation 0,10,20,30,40,50,60,70,80,90,100)

Secondary

MeasureTime frameDescription
analgesic drugstotal dose of analgesic drugs required at twenty four hours will be evaluatedanalgesic drugs given according to the routine practice in the ward
postoperative major morbiditiesat postoperative first, sixth, twelfth and twenty-forth hourspostoperative Myocardial Infarction (MI), Acute Kidney Injury(AKI), and Cerebrovascular Events (CVO)s.

Other

MeasureTime frameDescription
postoperative side effectsat postoperative first, sixth, twelfth and twenty-forth hoursnausea, vomiting, abdominal pain, agitation, head ache, muscular weakness, dizziness,hiccups, bronchospasm, bradycardia, itching, urinary retention,

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026