Intraoperative Blood Loss

3

Review clinical trials related to Intraoperative Blood Loss. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Effect of Obesity Phenotype on Intraabdominal Pressure and Bleeding in Major Lumbar Spinal Surgery

Obesity is prevalent among patients with lumbar degenerative disease and is a known risk factor for perioperative complications in spinal surgery. However, most existing evidence relies solely on body mass index (BMI) without distinguishing between central and peripheral obesity phenotypes. Central and peripheral fat distribution may have distinct biomechanical and hemodynamic consequences, particularly with respect to intraabdominal pressure (IAP) changes during prone positioning and intraoperative blood loss. This prospective single-center observational study aims to evaluate the effect of obesity phenotype - classified as non-obese, centrally obese, or peripherally obese based on BMI and waist-to-hip ratio - on intraabdominal pressure, intraoperative blood loss, and other perioperative outcomes in adult patients undergoing major lumbar spinal surgery (decompression and/or instrumentation)

Participants needed: 90
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Marmara University Pendik Training and Research HospitalUpdated: Jul 7, 2026
Eligibility criteria

Age 18-80 years [+4]

- Pediatric patients (<18 years) [+7]

Status: Recruiting

Topical Tranexamic Acid to Reduce Blood Loss During Cesarean Delivery

The goal of this clinical trial is to learn whether applying topical tranexamic acid (TXA) directly to the uterine incision during cesarean delivery can reduce surgical bleeding compared to placebo. The study will include pregnant women aged 18-51 undergoing elective cesarean delivery at term (37 weeks or more). The main questions it aims to answer are: * Does topical TXA shorten uterine closure time? * Does topical TXA reduce the need for additional hemostatic sutures? Researchers will compare women receiving topical TXA to those receiving placebo (normal saline) to see if TXA reduces intraoperative bleeding and improves surgical outcomes. Participants will: * Be randomly assigned to receive either topical TXA or placebo during cesarean delivery. * Have standard surgery and postoperative care identical in both groups. * Provide routine clinical data, including hemoglobin levels and recovery outcomes, from their medical records.

Participants needed: 112
Trial details
Phase: Early Phase 1Age: 18-51Biological sex: FemaleType: InterventionalSponsor: Wolfson Medical CenterUpdated: Jul 2, 2026Locations: 4
Eligibility criteria

Women aged 18 to 51 years [+6]

Known allergy or hypersensitivity to tranexamic acid (TXA) [+8]

Status: Recruiting

Tranexamic Acid in Pediatric Undergoing Proximal Femoral Osteotomies and/or Acetabular Osteotomy

Surgical hip reconstruction reduces the hip joint through soft tissue releases and osteotomies of the femur and/or pelvis. Blood loss and subsequent blood transfusion are normal consequences of hip reconstruction.

Participants needed: 400
Trial details
Age: 1-18Biological sex: AllType: InterventionalSponsor: Assiut UniversityUpdated: Nov 17, 2025Locations: 1
Eligibility criteria

ASA I - II [+1]

Patient's guardian refusal to participate in the study. [+4]