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Analysis of the Association Between Relevant Body Fluid Indicators at Admission and Perioperative Infections in Gynecological Inpatients

Analysis of the Association Between Relevant Body Fluid Indicators at Admission and Perioperative Infections in Gynecological Inpatients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109775
Enrollment
Unknown
Registered
2025-09-24
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Uterine Fibroids

Interventions

Observation group (Patients with infection events during the perioperative period):None
Control group (Patients without infection events during the perioperative period):None

Sponsors

Affiliated Hospital of Guangdong Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion Criteria:?? Females aged 18–65 years meeting indications for gynecological surgery (e.g., myomectomy, total hysterectomy, etc.). No preoperative evidence of infection (e.g., respiratory, urinary, or reproductive tract infections), with normal laboratory results (complete blood count, urinalysis, C-reactive protein [CRP], etc.). ?2. Surgical Requirements:?? Patients undergoing gynecological surgery (laparotomy, laparoscopy, or hysteroscopy) with an operative duration >= 30 minutes. Postoperative hospital stay >= 3 days to facilitate infection monitoring. ?3. Ethics and Informed Consent:?? All participants provided written informed consent, and the study was approved by the hospital’s Institutional Review Board (IRB).

Exclusion criteria

Exclusion criteria: 1.Comorbidities Interference:?? Severe cardiac, hepatic, or renal dysfunction; 2.Immunodeficiency (e.g., HIV-positive status, long-term immunosuppressant use) or coagulation disorders. ?2. Infection-Related Exclusions:?? Uncontrolled preoperative infections (e.g., pneumonia, urinary tract infection) or latent infections. ?3. Special Population Exclusions:?? Pregnant or lactating women (potential impact on immune status). ?4. Obesity or Malnutrition:?? BMI >= 30 or malnourished patients (may confound infection risk analysis). ?5. Other Interfering Factors:?? Loss to follow-up or incomplete postoperative data. ?6. Prior Pelvic Interventions:?? History of pelvic surgery or radiotherapy (may alter local microenvironment).

Design outcomes

Primary

MeasureTime frame
Antimicrobial consumption (cumulative DDDs), length of hospital stay, and antimicrobial use density (DDD/100 patient-days) in patients with perioperative infections;Preoperative inflammatory markers;Preoperative metabolic and immune status;

Countries

China

Contacts

Public ContactGuo Chunlian

Affiliated Hospital of Guangdong Medical University

834711202@qq.com+86 151 0752 6477

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026