Ahmed 2014.

Methods	Prospective randomised trial, patients equally divided into 2 groups.
Participants	124 women undergoing CS.
Interventions	Intervention group ‐ 10 mg/kg TA 5 minutes before skin incision. Both groups received 10 unit of oxytocin and 1 mL of ergometrine after delivery of the baby.
Outcomes	Blood loss from placental delivery till the end of surgery and from the end of surgery until 2 hours postpartum, haemoglobin and haematocrit levels on day 3 postpartum, maternal and neonatal adverse effects.
Notes	Blood loss 391 mL in intervention groups versus 597 mL in control group. Published in abstract form only. Unable to contact the authors to get more information. The abstract does not contain sufficient information on study design (randomisation, allocation concealment) for appraisal. Awaiting full publication of the study at this stage.