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Immune-Nutritional Scores and Sleep Quality After Total Abdominal Hysterectomy

I

Istinye University

Status

Not yet enrolling

Conditions

Postoperative Sleep Quality
Immune-Nutritional Indexes (PNI, HALP)

Treatments

Other: Immune-Nutritional Scoring and Postoperative Sleep Assessment

Study type

Observational

Funder types

Other

Identifiers

NCT07038564
TAH PNI HALP

Details and patient eligibility

About

This prospective observational study aims to evaluate the relationship between preoperative immune-nutritional status and postoperative sleep quality in women undergoing total abdominal hysterectomy under general anesthesia. Immune-nutritional scores, including the Prognostic Nutritional Index (PNI) and Hemoglobin-Albumin-Lymphocyte-Platelet (HALP) score, will be calculated using routine preoperative blood parameters. Postoperative sleep quality will be assessed using the Richards-Campbell Sleep Questionnaire (RCSQ). Secondary outcomes include postoperative pain scores and patient satisfaction. The study will enroll 60 patients and seeks to determine whether preoperative physiological markers can predict subjective recovery parameters such as sleep and comfort, potentially contributing to personalized perioperative care.

Enrollment

60 estimated patients

Sex

Female

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

0

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Central trial contact

ilke dolgun

Data sourced from clinicaltrials.gov

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