The goal of the clinical trial is to determine the effect of second-stage warm compress application on perineal pain and trauma among primiparous women. The main questions may reveal the pain intensity and the perineal outcome of the warm compress which might be helpful to the women during labor and related authority of the hospital. The intervention with warm perineal compression will be done among primiparous mothes during second stage of labor
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level of pain intensity
Timeframe: 15 minutes after application of warm compression
Perineal outcomes
Timeframe: 1 hour after application of warm compression