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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported