Weight Loss Following an Episode of Pre-eclampsia Using a Dissociated or Hypocaloric Diet in Overweight or Obese Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorCentre Hospitalier le Mans

About this trial

In view of the known link between pre-eclampsia, overweight/obesity and chronic kidney disease, the aim is to offer for obese and overweight patients to reduce their BMI without reducing lean body mass.

The POPADIPE project will make it possible to limit overweight or obesity by means of nutritional management chosen by the patient (hypocaloric or a dissociated diet). The latter has been the subject of little scientific investigation, particularly in relation to the management of post-pre-eclampsia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Person affiliated to social security

Free, informed and written consent signed by the participant and the investigator (no later than the day of day of inclusion and before any examination required by the research)

Patient over 18 years of age at the time of inclusion and < 45 years of age

Having had an pre-eclampsia in the last 5 years according to the definitions of the ISSHP 2018

Disqualifiers

Patients with a mental disability or language barrier that prevents them from understanding or consenting to the study

Patients deprived of their liberty by judicial or administrative decision

Patients under psychiatric care

Patients subject to a legal protection measure

Trial design

Design model

Parallel

Treatments tested in this trial

  • Hypocaloric diet

    Other intervention

    Hypocaloric diet

  • Dissociated diet

    Other intervention

    Dissociated diet

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: control groupPlacebo comparator 1 intervention
Group B: innovative groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Demonstrate Efficiency of personalised dietary management on weight loss in patients with a history of pre-eclampsia

Efficiency is evaluated by weight measurement

Time frame
1 year after care

Secondary outcomes

Other outcomes

Sponsors and contacts

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