se of acupuncture for the reduction of hospital admissions in the induction of labor due to chronologically prolonged gestation.ACUPUNT STUDY

Phase 1

• Conditions: This Clinical Trial will evaluate the efficacy and safety of acupuncture to promote labor in pregnant women who need an induction at birth and thus be able to give answers to all these women who are increasingly seeking these therapies, such as acupuncture, pregnancy and Childbirth together with usual medical practice.; Therapeutic area: Health Care [N] - Health Services Administration [N04]

• Registration Number: EUCTR2017-000145-40-ES
• Lead Sponsor: montserrat zamora brito

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-07-04
• Last Update Posted: 2 October 2017

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Low- and medium-risk term pregnant women (not including pregnant
women under age 18, grade I heart disease, high multiparity, and insufficient gestational control) between 40-41 w
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 117
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Pregnant women who do not want to participate in the project.

* Mid-risk pregnant women out of the inclusion criteria, high and very high risk.

* Pregnant women who do not understand the language.

* Pregnant women whose delivery attendance is not going to be performed in our Hospital ( Clínic Hospital of Barcelone )

* Pregnant women with anomalous fetal presentations according to the ultrasound of the third trimester: transverse, oblique and breech.

* Premature rupture of membranes before initiating intervention.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified