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Recruiting NCT06857760

Effects of Three Different Methods Applied to Patients After Spine Surgery on Nausea, Thirst and Comfort

No phase Interventional Spinal Surgery

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Ice cube, Mouth wash, Menthol lozenge.
Who it may be relevant to
Registry conditions: Spinal Surgery. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The aim of this study was to determine the effects of postoperative methods on nausea, thirst and comfort levels of patients undergoing spinal surgery.

Detailed description

Within the scope of this randomized controlled study, it is aimed to evaluate the effectiveness of ice, mouthwash and menthol lozenge interventions to provide effects on postoperative nausea, thirst and comfort in patients undergoing spinal surgery

Interventions

  • Other Ice cube
    ıce cube
  • Other Mouth wash
    Mouth wash
  • Other Menthol lozenge
    menthol lozenge

Primary outcome measures

  • Nausea [Time frame: once before the application and 60, 120, 180 and 240 min. after arrival at the clinic]
  • Thirst [Time frame: once before the application and 60, 120, 180 and 240 min. after arrival at the clinic]
  • Comfort [Time frame: once before the application and 240 min. after arrival at the clinic]

Eligibility criteria

Inclusion criteria

  • Adult patients who underwent lumbar disc herniation (LDH) surgery
  • LDH surgery patients who recieve general anesthesia
  • The patients who were conscious
  • The duration of surgery is between 0-3 hours

Exclusion criteria

  • Patients who cannot understand and speak Turkish
  • Allergic patients to menthol
  • Patients who received spinal anesthesia
  • Patients with lesions on the oral mucosa and lips
  • Patients requiring intensive care after surgical intervention

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 1 center
  • Amasya Şerefeddin Sabuncuoğlu Hospital — Amasya

Identifiers

NCT: NCT06857760 · A.30.2.ODM.0.20.08/569-677

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗