Heart Bypass Surgery Clinical Trials

Clinical trials related to Heart Bypass Surgery Procedure

Early Postoperative Pain and Related Outcomes After Cardiac Surgery: A Retrospective Cohort Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This observational study will evaluate factors that may be associated with pain during the first 24 hours after open heart surgery. The study will include adult patients who underwent coronary artery bypass grafting (CABG), heart valve surgery, or combined cardiac surgery. Researchers will retrospectively review existing medical records to examine whether patient characteristics, preoperative anxiety and depression, and factors related to surgery and anesthesia are associated with postoperative pain. The study will also evaluate postoperative nausea and vomiting and the need for additional pain medication. No treatment or intervention will be assigned to participants as part of this study. Study data will be collected retrospectively from existing medical records.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥18 years

• Underwent open cardiac surgery, including coronary artery bypass grafting (CABG), valve surgery, or combined cardiac surgery

• Complete perioperative and postoperative pain data available in the medical records

Locations
Other Locations
Turkey
SBU Antalya Training and Research Hospital
RECRUITING
Antalya
Contact Information
Primary
Meltem Ceylan Delice, MD
ceylanmeltem93@gmail.com
+905532705216
Time Frame
Start Date: 2026-08-10
Estimated Completion Date: 2026-09-07
Participants
Target number of participants: 99
Treatments
Cardiac Surgery Cohort
Adult patients who underwent open cardiac surgery, including coronary artery bypass grafting (CABG), valve surgery, or combined cardiac surgery, between April 1, 2025 and April 1, 2026. Existing medical records will be retrospectively reviewed to evaluate early postoperative pain and related outcomes. No study-specific treatment or intervention will be assigned by the investigators.
Related Therapeutic Areas
Sponsors
Leads: Meltem Ceylan Delice

This content was sourced from clinicaltrials.gov