Cesarean Section Surgery

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Review clinical trials related to Cesarean Section Surgery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Rivaroxaban vs Enoxaparin After Cesarean Section: Laboratory Thromboprophylaxis Outcomes

Pregnancy and the postpartum period increase venous thromboembolism (VTE) risk. After cesarean section, low-molecular-weight heparin (LMWH; enoxaparin) is commonly used for short-term thromboprophylaxis, but it requires daily subcutaneous injections and can cause adverse effects. Direct oral anticoagulants (DOACs) such as rivaroxaban offer convenient once-daily oral dosing. In women who meet institutional criteria for short-term postpartum thromboprophylaxis until hospital discharge, we will compare the laboratory anticoagulant effect of rivaroxaban versus enoxaparin using thrombin generation parameters. This randomized, open-label trial will enroll women undergoing elective cesarean section who are indicated for in-hospital prophylaxis. Blood will be drawn on postoperative day 2 at trough (pre-dose) and peak (\~3 hours post-dose) to measure thrombin generation, anti-Xa activity and drug levels, and participants will complete the Anti-Clot Treatment Scale (ACTS) satisfaction questionnaire. Safety follow-up will occur by telephone at 2 days post-discharge and at 6 weeks postpartum.

Participants needed: 62
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Wolfson Medical CenterUpdated: Sep 15, 2026Locations: 1
Eligibility criteria

Hebrew-speaking women [+3]

Known thrombophilia [+14]

Status: Not yet recruiting

Role of Intravenous Calcium to Decrease Blood Loss During Intrapartum Cesarean Section

To determine the effectiveness of prophylactic intravenous calcium chloride administered after cord clamping in reducing postpartum blood loss during intrapartum cesarean section.

Participants needed: 182
Trial details
Phase: Phase 2Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Pak Emirates Military HospitalUpdated: Apr 24, 2026Locations: 1
Eligibility criteria

Women aged 18-45 years undergoing intrapartum cesarean section at ≥34 weeks of g... [+2]

Known bleeding disorders or preoperative coagulation abnormalities [+5]

Status: Recruiting

Analysis of the Incidence and Risk Factors of Chronic Pain After Cesarean Section

Persistent postoperative pain is a globally recognized issue that deserves attention. Cesarean section is one of the surgeries that may cause persistent postoperative pain. PSPP may affect communication between mother and baby, and may lead to postpartum depression, which has a negative impact on the daily activities and quality of life of mothers. It is an important clinical issue. The main purpose of this study is to (1) prospectively investigate the overall incidence and characteristics of persistent pain after cesarean section at 3, 6, and 12 months after surgery; (2) Use regression analysis and data modeling analysis to evaluate the relationship between perioperative variables and chronic pain in postpartum women undergoing cesarean section; (3) Analyze the relationship between chronic pain after cesarean section and postpartum depression in postpartum women.

Participants needed: 600
Trial details
Age: 20-50Biological sex: FemaleType: ObservationalSponsor: Huazhong University of Science and TechnologyUpdated: Nov 26, 2024Locations: 1
Eligibility criteria

Age range from 20 to 50 years old; [+3]

Have a history of dementia, mental illness, or any central nervous system disord... [+5]