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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04128033
Other study ID # 2018-A03070-55
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 4, 2019
Est. completion date July 1, 2019

Study information

Verified date October 2019
Source Centre Hospitalier Sud Francilien
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

During the study period, any patient who enters labour and reports to the maternity ward and meets the inclusion and non-inclusion criteria is offered to participate in the study by the midwife acupuncturist present.

After signing the informed consent, a numbered envelope with the randomization arm is assigned to the patient. The acupuncturist midwife does not perform the delivery herself. At the time of the expulsive efforts, she punctures the point drawn at random. The patient's participation in the study ends when she leaves the labour room after the birth.


Description:

During the study period, any patient who enters labour and reports to the maternity ward and meets the inclusion and non-inclusion criteria is offered to participate in the study by the midwife acupuncturist present. She's responsible for explaining the purpose and practicalities of the study orally and issues a written information document. The information provided is the same regardless of the midwife present. If she agrees to participate in the study, the patient signs the consent form.

After signing the informed consent, a numbered envelope with the randomization arm is assigned to the patient. The acupuncturist midwife does not perform the delivery herself. At the time of the expulsive efforts, she punctures the point drawn at random. She collects the clinical Research Form from the time the patient signs the consent form until she leaves the labour room after the birth.

The patient's participation in the study ends when she leaves the labour room after the birth. No further follow-up is planned.


Recruitment information / eligibility

Status Completed
Enrollment 350
Est. completion date July 1, 2019
Est. primary completion date July 1, 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- primiparous or multiparous women who have never given birth vaginally

- term patients (after 37 weeks of amenorrhea)

- patients delivering a fetus in cephalic presentation

- patients speaking and understanding French.

Exclusion Criteria:

- patients suspected of having a fetal macrosomy (greater than the 97th percentile) on the last ultrasound

- patients with twin pregnancies

- excised patients

- patient who has made an acupuncture preparation during pregnancy

- patients with fetal death in utero

- patients requiring medical termination of pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Puncture of the RP6 point
Puncture of RP6 "San Yin Jiao" point, located just behind the posterior edge of the tibia 3 cm above the end of the inner malleolus.
Puncture of the placebo point
Puncture of a placebo point "outside the meridian", with no effect

Locations

Country Name City State
France Centre Hospitalier Sud Francilien Corbeil-Essonnes

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Sud Francilien

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of intact perineum after childbirth Rate of intact perineum after childbirth immediately after childbirth
Secondary Rate of simple perineal tears lesion of the skin, vaginal mucosa, connective tissue, or sometimes the superficial muscle plane immediately after childbirth
Secondary Rate of complete perineal tears Sphincter damage to the anus immediately after childbirth
Secondary Rate of complicated complete perineal tears Damage to the anal mucosa immediately after childbirth
Secondary Rate of episiotomies performed Rate of episiotomies performed immediately after childbirth
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