Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
NCT06067906

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

Led by Centre Hospitalier le Mans · Updated on 2024-08-28

60

Participants Needed

1

Research Sites

261 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 45Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Person affiliated to social security
  • Signed free, informed, and written consent before any study examination
  • Female patient aged over 18 and under 45 years at inclusion
  • History of pre-eclampsia in the last 5 years according to ISSHP 2018 definitions
  • BMI between 25 kg/m² and 40 kg/m² and acceptance of dietetic follow-up
  • Medical prescription for dietetic follow-up aimed at weight loss
  • Balanced diet at study entry
Not Eligible

You will not qualify if you...

  • Mental disability or language barrier preventing understanding or consenting
  • Deprivation of liberty by judicial or administrative decision
  • Under psychiatric care
  • Subject to legal protection measures
  • Cognitive disorders or defined eating disorders
  • Pregnant or breastfeeding
  • Undergoing steroid treatment and/or immunosuppression
  • On low-calorie or dissociated diet for at least 6 months
  • Chronic kidney disease stage 3A or higher

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Du Mans

Le Mans, France, 72000

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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