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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05106738
Other study ID # Policlinic hospital, 9
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2021
Est. completion date November 30, 2023

Study information

Verified date December 2023
Source University of Bari
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Phase angle (PhA) is a biometric parameter measured by bioimpedance analysis (BIA), which reflects organism cellularity and tissues hydration. In addition, since it correlates with the presence of inflammation and the nutritional status, it could be useful to monitor inflammatory bowel disease (IBD) activity. The aim of this study was to establish the potential use of PhA as a new non-invasive and sensitive marker correlated with mucosal healing and/or IBD activity.


Description:

Currently, fecal calprotectin is considered the best indirect marker inversely correlated with the mucosal healing in patients with inflammatory bowel disease (IBD). C reactive protein (CRP), is less reliable than fecal calprotectin in the evaluation of IBD activity. In order to establish the potential use of phase angle (PhA) as a new non-invasive and sensitive marker of mucosal healing and/or disease activity in patients with IBD, patients with diagnosis of chronic inflammatory bowel diseases (IBD) according to the European Crohn's and Colitis Organization (ECCO) guidelines will be enrolled. In these patients, the following parameters will be evaluated: age, sex, body mass index (BMI), percentage of weight loss in the last 6 months, duration of illness, location of disease, any previous intestinal surgery, ongoing therapy for IBD, activity disease by clinical scores, CRP, fecal calprotectin, disease activity by endoscopic scores, PhA and fat free mass (FFM).


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date November 30, 2023
Est. primary completion date October 31, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - histological report confirming the diagnosis of IBD, - value of C-reactive protein (CRP) - fecal calprotectin, - colonoscopy within 3 months from the enrollment. Exclusion Criteria: - presence of ascites or edema, - chronic or autoimmune inflammatory diseases, - ongoing infections, - recent surgery (in the last 6 months), - neoplastic diseases, - ongoing enteral or parenteral nutrition, - presence of fistulae, - ileostomy or colostomy, - short bowel syndrome, - pregnancy or lactation.

Study Design


Locations

Country Name City State
Italy Michele Barone Bari BA

Sponsors (1)

Lead Sponsor Collaborator
University of Bari

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary The correlation of phase angle with mucosal healing in patients with inflammatory bowel disease The evaluation of phase angle (PhA), expressed in degrees, will be obtained by bioimpedenziometry, using a specific software (Bodygram Pro 3.0, Akern srl, Pontassieve, Italy). The assessment of mucosal healing will be performed by the following endoscopic scores: the Simple Endoscopic Score for Crohn's Disease (SES-CD) and the Mayo endoscopic score for Crohn's disease and Ulcerative Colitis (UC), respectively. At enrollment
Secondary Evaluation of the presence of malnutrition by bioimpedance analysis Malnutrition will be assessed by the evaluation of body composition [fat free mass (FFM) and fat mass (FM) expressed in kg], by bioimpedance analysis At enrollment
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