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Apgar Score clinical trials

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NCT ID: NCT06297031 Completed - Labor Pain Clinical Trials

Heat Application to the Sacral Region and Pain Level During the First Stage of Labor

Start date: April 1, 2020
Phase: N/A
Study type: Interventional

The aim of this study was to determine the effect of hot application applied to the sacral region during first stage of labor on women's pain level and labor process.

NCT ID: NCT04104009 Recruiting - Mental Health Issue Clinical Trials

The Relation Between Midwifery Education and Listening to Classical Music With the Mode of Delivery

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

The emotional and psychological well-being of women influence the perception and experience of pregnancy and childbirth. Pregnant women with a fear of childbirth are more likely to give birth by caesarean section. An increased risk of obstetric interventions such as planned and emergency caesarean section has been determined. Childbirth education is an intervention that has a major impact on maternity outcomes and birth experience

NCT ID: NCT01255839 Completed - Caesarean Section Clinical Trials

The Balloon Project for Birth Induction

Start date: December 2002
Phase: Phase 4
Study type: Interventional

The use of prostaglandin E2 (PGE2) for induction of labour in women with unfavourable cervices is well-established1. There are, however, potential side effects to prostaglandins, in particular the risk of uterine hypertonicity which may affect fetal outcome. In theory a mechanical ripening based on dilatation of the cervix as well as induction of production of endogenous prostaglandin has potentially less influence on the fetal outcome but a Cochrane review from 2001 scrutinized studies on mechanical ripening versus placebo/no treatment or prostaglandin E2. They conclude there is insufficient data to evaluate the effectiveness in terms of likelihood of vaginal delivery in 24 hours, and emphasise the need for large sample size studies and substantive outcomes. Two later randomised studies compared mechanical ripening to PGE2 and found discrepant results regarding time from induction to delivery. The primary purpose of the present study was in a randomized design to compare the efficacy of double-balloon catheter versus vaginal PGE2 (minprostin 3 mg) on induction of labour, duration of birth and fetal outcome. Secondary analyses were to evaluate the results for various subgroups, i.e. primipara/multipara, gemelli, vaginal birth after caesarean, preterm birth and intra uterine growth restriction.

NCT ID: NCT01186627 Recruiting - Premature Birth Clinical Trials

Trial to Evaluate a Specified Type of Apgar (TEST-APGAR) Follow Up Study

Start date: April 2010
Phase: N/A
Study type: Observational

A specified version of the Apgar-Score, that can be used in newborns under resuscitation, was developed and its value to predict chronic damage in preterm infants will be tested.