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Strategy of Micronutrient Management in Parturient and Layered Women With a Dietary Supplement Rich in Porphyra HSP®

NCT02967796 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2018-07-17

No results posted yet for this study

Summary

The aim of the study is to evaluate in primiparous patients the benefit of supplementation with Proteochoc® to reduce perineal pain in the postpartum especially, in sitting posture. The patient is followed from the delivery to 6 to 8 weeks after.

Conditions

  • Postpartum Perineal Pain

Interventions

DIETARY_SUPPLEMENT

Proteochoc

Sponsors & Collaborators

  • PiLeJe

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-04
Primary Completion
2017-04-25
Completion
2017-04-25

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02967796 on ClinicalTrials.gov