About this trial
This prospective observational study investigates the impact of preoperative regional anesthesia on postoperative sleep quality in patients undergoing mastectomy. Sleep quality will be assessed using two validated tools: the Richards-Campbell Sleep Questionnaire (RCSQ) for all participants, and the Pittsburgh Sleep Quality Index (PSQI) in a subgroup. The study also examines the relationship between sleep quality and postoperative pain, patient satisfaction, and psychological status measured by the Hospital Anxiety and Depression Scale (HADS). Patients will be grouped based on anesthesia technique-general anesthesia alone or general anesthesia combined with regional block-and sleep outcomes will be compared. The study aims to provide evidence on how anesthetic technique and psychological factors affect recovery and sleep quality after breast cancer surgery.
Eligibility criteria
Qualifiers
Female patients aged 18 years or older
Undergoing elective mastectomy surgery
ASA physical status I to III
Willing and able to provide written informed consent
Disqualifiers
History of major psychiatric or neurological disorders
Regular use of antidepressants, anxiolytics, or hypnotics
Difficult airway management during anesthesia (e.g., intubation or ventilation complications)
Reoperation within the first 24 hours after surgery
Trial design
Treatments tested in this trial
- Regional Analgesic Block
Treatment groups
Locations
Sponsors and collaborators
Istinye University
Lead sponsor
Haseki Training and Research Hospital
Sponsor institution