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Search / Trial NCT07038564

Immune-Nutritional Scores and Sleep Quality After Total Abdominal Hysterectomy

Launched by ISTINYE UNIVERSITY · Jun 18, 2025

Trial Information

Current as of June 28, 2025

Not yet recruiting

Keywords

ClinConnect Summary

This clinical trial is studying how a woman’s immune and nutritional health before surgery might affect how well she sleeps after having a total abdominal hysterectomy—a surgery to remove the uterus. Researchers will look at simple blood test results taken before surgery to calculate immune-nutritional scores and then see if these scores relate to how patients sleep after the operation. They will also check pain levels and how satisfied patients feel with their recovery. The goal is to understand if these pre-surgery health markers can help predict recovery experiences like sleep quality and comfort, which could lead to more personalized care during and after surgery.

Women between 18 and 70 years old who are having an elective (planned) total abdominal hysterectomy under general anesthesia may be eligible to join. To participate, patients need to have routine blood tests done before surgery, plan to stay at least one night in the hospital afterward, and be able to understand and complete simple questionnaires about their sleep and recovery. Women with certain health conditions like sleep disorders, mental illness, or those taking sleep medications won’t be eligible. If you join, you can expect to have your blood test results reviewed before surgery, then be asked about your sleep and pain after surgery using easy questionnaires. This study is not yet recruiting participants.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Female patients aged 18-70
  • ASA physical status I-III
  • Undergoing elective total abdominal hysterectomy under general anesthesia
  • Available complete blood count and biochemistry results within 24 hours preoperatively
  • Planned to stay at least one night postoperatively
  • Sufficient cognitive ability to understand and complete questionnaires
  • Provided written informed consent
  • Exclusion Criteria:
  • History of neurological or psychiatric illness
  • Diagnosed sleep disorders
  • Current use of sedative or hypnotic medications
  • Undergoing additional surgical procedures during operation
  • Requiring postoperative intensive care
  • Operated under spinal or epidural anesthesia

About Istinye University

Istinye University is a leading academic institution committed to advancing medical research and education. With a strong emphasis on innovation and collaboration, the university actively engages in clinical trials that aim to enhance healthcare outcomes and contribute to scientific knowledge. Leveraging its state-of-the-art facilities and a team of experienced researchers and clinicians, Istinye University fosters a rigorous environment for conducting high-quality clinical studies across various medical disciplines. The institution is dedicated to ethical practices and patient safety, ensuring that all research initiatives align with the highest standards of integrity and scientific excellence.

Locations

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported