Strategy of Micronutrient Management in Parturient and Layered Women With a Dietary Supplement Ri… (NCT02967796) | Clinical Trial Compass
CompletedNot Applicable
Strategy of Micronutrient Management in Parturient and Layered Women With a Dietary Supplement Rich in Porphyra HSP®
France60 participantsStarted 2015-09-04
Plain-language 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.
Who can participate
Age range
18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.