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Instrumental Delivery clinical trials

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NCT ID: NCT01261689 Completed - Analgesia, Epidural Clinical Trials

The Randomised Epidural Analgesia in Term Delivering Women Trial (TREAT)

TREAT
Start date: September 2008
Phase: N/A
Study type: Interventional

* The objective of the study: to assess the impact of a proactive policy of offering EA at the start of labour as compared to a restrictive policy or care as usual. * Study design: It concerns a multicentre randomised open label trial. * Study population: Term nulliparous and multiparous women with a child in cephalic presentation, and without contraindications for vaginal labour or EA. * Intervention: Women will be allocated to the EA group or the care-as-usual group. In the EA group, women are given an EA as soon as they are in labour. In the care-as-usual (restrictive) group, women receive pain relief only on their explicit request.