An observational study in Femoral Neck Fractures, Blood Loss, Surgical and Postoperative Pain, sponsored by Bursa Yuksek Ihtisas Training and Research Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2026-10-07.
Sponsored by Bursa Yuksek Ihtisas Training and Research Hospital · Observational
This retrospective observational study evaluates the effect of different regional anesthesia techniques on perioperative blood loss in patients undergoing femoral neck fracture surgery. Patients who received tranexamic acid were grouped by anesthesia method (lumbar plexus block, spinal anesthesia, or general anesthesia). The primary outcomes were intraoperative blood loss and the change in hemoglobin between the preoperative and postoperative periods. Secondary outcomes were postoperative pain (VAS) and total analgesic consumption during the first 24 hours.
204 studies on the registry are indexed under Femoral Neck Fractures; 41 are open to participants now.
This study's enrollment of 150 is above the median of 134 across 59 observational studies indexed under Femoral Neck Fractures.
Browse Femoral Neck Fractures studies →Bursa Yuksek Ihtisas Training and Research Hospital is the lead sponsor of 46 studies on the registry; 19 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Patients aged 18-100 years who underwent femoral neck fracture surgery and received tranexamic acid, identified by retrospective chart review
Exclusion Criteria:
Patients who received lumbar plexus block plus tranexamic acid.
Patients who received spinal anesthesia combined with tranexamic acid.
Patients who received general anesthesia combined with tranexamic acid.
Intraoperative blood loss
Intraoperative blood loss estimated from the volume in the aspirator container and the blood absorbed in surgical sponges
Time frame: Intraoperative (during surgery)
Change in hemoglobin level
Difference between preoperative and postoperative hemoglobin concentration (g/dL)
Time frame: Preoperative and within 24 hours postoperatively
Postoperative pain score (VAS)
Postoperative pain assessed using the Visual Analog Scale (VAS), ranging from 0 (no pain) to 10 (worst pain); higher scores indicate worse pain.
Time frame: 2, 6, 12 and 24 hours postoperatively
Total analgesic consumption
Total amount of analgesic consumed in the first 24 postoperative hours
Time frame: First 24 hours postoperatively
Plan to share: No — Individual participant data will not be shared.
No publications or documents are linked to this record.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.
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Bursa Yuksek Ihtisas Training and Research Hospital