Recruiting NA Prader-Willi Syndrome

New treatment option for Prader-Willi Syndrome

Official title The Intervention of Obesity in Children With Prader-Willi Syndrome Using Prebiotics and Probiotics

ClinicalTrials.gov ID: NCT05791604

What this study is testing

What it's testing
Prader-Willi syndrome (PWS) is a rare genetic disease, with hyperappetite and severe obesity. At present, there is no effective drugs and interventions to help control the appetite of PWS patients.
  • You might receive a placebo (an inactive treatment) instead of the study drug.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 3 to 10

You may be able to join if

  • Pre-adolescent children with Prader Willi syndrome which were definitely diagnosed by gene testing.
  • Consistent with the diagnostic criteria for obesity.
  • Not participate in other research projects at present or three months before the research;
  • Agree to participate in the test and obtain the consent of their parents; voluntarily be the people and sign the informed consent form.

You likely can't join if

  • Losing weight in ways other than the intervention measures of this project, such as taking weight loss drugs or known drugs that cause weight change;
  • Use antibiotics within 1 month before the study and lasted for 3 days or more;
  • Use probiotics within 1 month before the study and lasted for 3 days or more;
  • Complicated with liver and renal insufficiency (alanine aminotransferase and serum creatinine indexes exceed 2 times the upper limit of the normal...
  • Have gastrointestinal diseases affecting food digestion and absorption (such as severe diarrhea, constipation, severe gastrointestinal inflammation...
  • Surgery was performed within 1 year before the study (except for appendicitis and hernia surgery);
See the full eligibility criteria
Who can join
  • Pre-adolescent children with Prader Willi syndrome which were definitely diagnosed by gene testing.
  • Consistent with the diagnostic criteria for obesity.
  • Not participate in other research projects at present or three months before the research;
  • Agree to participate in the test and obtain the consent of their parents; voluntarily be the people and sign the informed consent form.
What rules you out
  • Losing weight in ways other than the intervention measures of this project, such as taking weight loss drugs or known drugs that cause weight change;
  • Use antibiotics within 1 month before the study and lasted for 3 days or more;
  • Use probiotics within 1 month before the study and lasted for 3 days or more;
  • Complicated with liver and renal insufficiency (alanine aminotransferase and serum creatinine indexes exceed 2 times the upper limit of the normal value set by the hospital);
  • Have gastrointestinal diseases affecting food digestion and absorption (such as severe diarrhea, constipation, severe gastrointestinal inflammation, active gastrointestinal ulcer, acute cholecystitis, etc.); severe...
  • Surgery was performed within 1 year before the study (except for appendicitis and hernia surgery);
  • Have hepatitis B, active tuberculosis, AIDS and other infectious diseases;
  • Those who are suffering from mental illness and are taking psychotropic drugs such as antidepressants.

The study team makes the final eligibility decision.

Where it's taking place

  • Shanghai, Shanghai Municipality, China

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 3 years to 10 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Shanghai, Shanghai Municipality, China. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.