TrialX
Image

A Non-Interventional Pilot Study to Explore the Role of Gut Flora in IBS

A Non-Interventional Pilot Study to Explore the Role of Gut Flora in IBS

Recruiting
100 years and younger
All
Phase N/A

Overview

This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records.

Description

The goal of this Research Study is to better understand how the genetic information in subject's microbiome correlates to IBS.

Eligibility

Inclusion Criteria:

  1. Signed informed consent, demonstrating that the patient understands the procedures required for the study and the purpose of the study
  2. May be signed by parent or legal guardian in the case of minor or adult unable to provide consent
  3. Male or female of all ages
  4. Diagnosis of IBS

Exclusion Criteria:

  1. Refusal to sign informed consent form
  2. History of bariatric surgery, total colectomy with ileorectal anastomosis or proctocolectomy.
  3. Postoperative stoma, ostomy, or ileoanal pouch
  4. Participation in any experimental drug protocol within the past 12 weeks
  5. Treatment with total parenteral nutrition

Study details
    Irritable Bowel Syndrome
    Irritable Bowel Syndrome With Diarrhea
    Irritable Bowel Syndrome Mixed
    Irritable Bowel Syndrome With Constipation
    Irritable Bowel Syndrome Without Diarrhea
    Irritable Bowel Syndrome Aggravated
    Irritable Bowel Syndrome Characterized by Constipation
    Irritable Bowel Syndrome Characterised by Alternating Bowel Habit

NCT04214470

ProgenaBiome

16 February 2024

Contact a study center
Step 1 Get in touch with the nearest study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team

Email

View email

Phone

Phone country flag

View phone
Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.