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Clinical Trial NCT06857760 for Spinal Surgery is recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here.
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Effects of Three Different Methods Applied to Patients After Spine Surgery on Nausea, Thirst and Comfort 128

Recruiting
Clinical Trial NCT06857760 is an interventional study for Spinal Surgery that is recruiting. It started on 21 February 2025 with plans to enroll 128 participants. Led by Ondokuz Mayıs University, it is expected to complete by 30 December 2026. The latest data from ClinicalTrials.gov was last updated on 4 March 2025.
Brief Summary
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
Official Title

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

Conditions
Spinal Surgery
Other Study IDs
  • A.30.2.ODM.0.20.08/569-677
NCT ID Number
NCT06857760
Start Date (Actual)
2025-02-21
Last Update Posted
2025-03-04
Completion Date (Estimated)
2026-12-30
Enrollment (Estimated)
128
Study Type
Interventional
PHASE
N/A
Status
Recruiting
Keywords
nausea, thirst, comfort
Primary Purpose
Supportive Care
Design Allocation
Randomized
Interventional Model
Parallel
Masking
Double
Arms / Interventions
Participant Group/ArmIntervention/Treatment
No InterventionControl group
Routine care
N/A
ExperimentalIce cube
Ice cube
ıce cube
ExperimentalMouth wash
Mouth wash
Mouth wash
ExperimentalMenthol lozenge
Menthol lozenge
menthol lozenge
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Nausea
Nausea level: It consists of a numeric scale. Among the numbers, ''0'' corresponds to ''no thirst/nausea'' and ''10'' corresponds to ''very much thirst/nausea''. As the number increases, nausea and thirst will be accepted as increased. There is no cut-off point.
once before the application and 60, 120, 180 and 240 min. after arrival at the clinic
Thirst
Thirst level: A minimum score of 12 and a maximum score of 60 can be obtained from the scale. The higher the score obtained from the scale, the higher the level of thirst discomfort of the patients.
once before the application and 60, 120, 180 and 240 min. after arrival at the clinic
Comfort
Comfort level: The highest score that can be obtained from the scale is 192 and the lowest score is 48. A high SCS scoring indicates a high comfort level of the individual.
once before the application and 240 min. after arrival at the clinic
Participation Assistant
Eligibility Criteria

Eligible Ages
Adult, Older Adult
Minimum Age
18 Years
Eligible Sexes
All
  • 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

  • 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
Ondokuz Mayıs University logoOndokuz Mayıs University
Study Responsible Party
Özge İşeri, Principal Investigator, Assistant Professor, Ondokuz Mayıs University
Study Central Contact
Contact: Özge İşeri Özge İşeri, Assistant Professor, PhD, 03623121919, [email protected]
Contact: Ayşe Kale Postgraduate doctorate student, RN, MSc, [email protected]
1 Study Locations in 1 Countries
Amasya Şerefeddin Sabuncuoğlu Hospital, Amasya, Turkey (Türkiye)
Recruiting