Sleep During Recovery: Effect of Preoperative Regional Block on Postoperative Sleep Quality in Mastectomy Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorIstinye University

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

66 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Istinye University

Lead sponsor

Haseki Training and Research Hospital

Sponsor institution