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Cervical Dystocia clinical trials

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NCT ID: NCT02394041 Terminated - Cervical Dystocia Clinical Trials

Randomised Controlled Trial of the Efficacy of Acupuncture Versus Placebo on the Caesarean Section Rate in Case of Cervical Dystocia in Full-term Pregnancy

ACUCESAR
Start date: November 2012
Phase: N/A
Study type: Interventional

The principal objective of the trial is to demonstrate that acupuncture could reduce the caesarean section rate for cervical dystocia. Secondary objectives: To demonstrate that acupuncture can: - reduce morbidity, fetal mortality and duration of childbirth; - reduce the cost of care, due to diminution of caesarean sections and duration of obstetric labor; - to evaluate the tolerance.