Descriptive Study About a Strategy of Micronutrient Management in Parturient and Layered Women With Proteochoc®, a Dietary Supplement Rich in Porphyra HSP®
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Postpartum Perineal Pain
- Sponsor
- PiLeJe
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- perineal pain intensity in the sitting position
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief 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.
Detailed Description
For this study, 60 patients are going to be included. There will be 2 groups : a supplemented one (proteochoc®) and a non supplemented one (control). The patients of these two groups will have the same follow-up At the time of inclusion, an inclusion card is completed describing the patient's socio-demographic characteristics, major medical, surgical and obstetric history. After an uncomplicated delivery, women stay in maternity for a maximum of 3 days. In accordance with standard medical practice, women will be seen daily from D0 to D + 3 by the nursing staff. The investigating physician and his team will complete the follow-up sheets in the aftermath (day1), day3 and 6-8 weeks after the usual visits. The data collected are information on medication treatments, prescribed care, assessment of the patient's overall condition and recovery, and monitoring of perineal lesions and complications if applicable. In the same time (day1, day3, day6, day14 and 6-8 weeks after, the patient will also complete a patient follow-up sheet to collect her impressions. The data collected are the medications taken, the care taken, the general pain felt, the perineal pain felt if applicable, and the fatigue felt.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Female aged over 18
- •First pregnancy
- •Having given birth, at a term greater than or equal to 37 SA, by low route, of a single child born alive and not hospitalized in the aftermath of immediate layers
- •For whom the investigator has freely decided to propose a complementation by Protéochoc® on the day of delivery and its sequences of layers
- •Having freely decided to buy Protéochoc® and follow the advice of consumption proposed by its gynecologist-obstetrician
- •Having agreed to sign a consent to participate in the investigation after receiving informed information from the investigator
Exclusion Criteria
- •Serious pathology running
- •Suffering before the pregnancy of any of the following conditions:
- •Chronic pelvic pain syndrome
- •Ilio-inguinal, ilio-hypogastric and genito-femoral pudendal neuralgia
- •Pains with osteo-ligamentary component: the syndrome of the dorsolumbar hinge and the coccygodynia
- •Myofacial Syndrome
- •Pain of muscular origin: the syndrome of the pyriform muscle, syndrome of the obturator muscle
- •Pains of venous origin: pelvic varices
- •Allergy to any of the components of Proteochoc®
- •Patient refusing to participate or unable to participate in the survey due to major language problems or major neuropsychiatric disorders
Outcomes
Primary Outcomes
perineal pain intensity in the sitting position
Time Frame: day 6
The primary outcome will be the perineal pain intensity in the sitting position measured by a visual analogue scale (rated 0 to 10) at day 6 in women who chose to complement versus women who did not wish to take the supplementation
Secondary Outcomes
- Patient's evaluation(Day 56)
- Doctor's evaluation(Day 56)