Randomized Controlled Trial on the Use of Pain Diary in Assessing Early Postoperative Pain Following Laparoscopic Cholecystectomy

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Turkey
Menteşe State Hospital
RECRUITING
Muğla
Contact Information
Primary
Muhammed A ASLAN
aslanmuhammed282@gmail.com
+905313769110
Time Frame
Start Date: 2025-11-15
Estimated Completion Date: 2027-01-30
Participants
Target number of participants: 142
Treatments
Experimental: Pain Management Intervention Group
Participants in this group will follow the pain management protocol after laparoscopic cholecystectomy, including recording postoperative pain in a pain diary.
No_intervention: Control Group
Participants in this group will receive standard care after laparoscopic cholecystectomy. Postoperative pain will be assessed using the Visual Analog Scale (VAS) at scheduled times by nurses and researchers, and recorded accordingly
Sponsors
Leads: Muğla Sıtkı Koçman University

This content was sourced from clinicaltrials.gov