Large cervical fibroids Pregnancy and Childbirth
Conditions
Interventions
This study does not involve active interventions as it is observational.
Participants and Study Design
This retrospective cohort study included 152 patients who underwent surgery for large cervical f
Sponsors
Science and Technology Department of Zhejiang Province
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Patients diagnosed with cervical fibroids by ultrasound, with a fibroid diameter of =8 cm 2. Age between 18 and 65 years 3. Availability of complete clinical data, including detailed preoperative examination results
Exclusion criteria
Exclusion criteria: 1.Presence of severe comorbidities, such as uncontrolled diabetes or severe cardiovascular or pulmonary diseases. 2.Patients who are pregnant or breastfeeding. 3.History of malignant uterine tumors. 4.Incomplete clinical data or missing preoperative examination results.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The following primary outcome measures are assessed using data collected in medical records at one timepoint: 1. Postoperative hospital stay duration measured in days 2. Time to first mobilization measured in hours 3. Postoperative pain scores measured using the Visual Analog Scale (VAS) 4. Postoperative complication rates e.g., infections, adhesions, or other surgical complications | — |
Secondary
| Measure | Time frame |
|---|---|
| The following secondary outcome measures are assessed using data collected in medical records at one timepoint: 1. Changes in Blood Biochemical Markers: 1.1. Preoperative and postoperative hemoglobin levels 1.2. White blood cell counts 1.3. Neutrophil ratio 1.4. C-reactive protein (CRP) 2. Intraoperative Metrics: 2.1. Intraoperative blood loss 2.2. The number of fibroids removed 3. Specific Recovery Milestones: 3.1. Time to first flatus (measured in hours) | — |
Countries
China
Contacts
Public ContactXiaoyong Li
Outcome results
None listed