Pain Diary Use After Laparoscopic Cholecystectomy
Randomized Controlled Trial on the Use of Pain Diary in Assessing Early Postoperative Pain Following Laparoscopic Cholecystectomy
Muğla Sıtkı Koçman University
142 participants
Nov 15, 2025
INTERVENTIONAL
Conditions
Summary
This randomized controlled study aims to evaluate the effectiveness of using a pain diary in the assessment of early postoperative pain in patients undergoing laparoscopic cholecystectomy. Patients will be randomly assigned to a pain diary group or a control group receiving routine pain assessment. Postoperative pain intensity will be measured at predefined time points using standardized pain assessment tools. The study seeks to improve patient participation in postoperative pain evaluation without introducing additional pharmacological interventions.
Eligibility
Inclusion Criteria10
- Admitted for elective laparoscopic cholecystectomy
- Scheduled for first-time laparoscopic cholecystectomy
- Aged 18 years or older
- Able to speak, read, and understand Turkish
- Literate
- Communicative and cooperative
- ASA score of 1, 2, or 3
- Expected to stay at least 24 hours in the hospital post-surgery
- Capable of understanding study instructions
- Willing to participate voluntarily
Exclusion Criteria9
- Prolonged stay in the recovery unit due to extended effects of general anesthesia
- Admission to intensive care unit postoperatively
- Having chronic pain and receiving treatment for it
- Being a cancer patient
- Having a writing disability
- Inability to communicate
- Having cognitive, affective, verbal, visual, or auditory impairments
- Diagnosed psychiatric disorders such as anxiety or depression and using related medications
- Choosing to withdraw from the study after giving consent
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Interventions
This pain management protocol is specifically tailored for patients undergoing laparoscopic cholecystectomy and combines both scheduled pharmacological analgesics and non-pharmacological pain control measures. Unlike other studies, it includes daily pain diary monitoring to objectively track patient-reported postoperative pain and recovery outcomes.
Locations(1)
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NCT07308730