Impact of Therapy Using Colesevelam Treatment Reducing Bile Acids in Patients With Fontan Circula… (NCT06197763) | Clinical Trial Compass
UnknownPhase 1/2
Impact of Therapy Using Colesevelam Treatment Reducing Bile Acids in Patients With Fontan Circulation.
50 participantsStarted 2024-06-01
Plain-language summary
This is the first pilot study proposing a novel therapeutic option treating patients with Fontan circulation (FC), a high-risk condition that has no definite treatment options available, other than heart or heart-liver transplantation. The investigator's identification of elevated BA and their association with adverse clinical - investigational features in Fontan patients are novel.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria - Fontan participants
i) Of full age of consent (at least ≥ 18 years of age) at screening
ii) Signed and dated written informed consent in accordance with ICF-GCP and local regulations prior to admission to the study
iii) Male or female participants. Women of childbearing potential (WOCBP) must be ready and able to use highly effective methods of birth control that result in a low failure rate of less than 1% per year when used consistently and correctly. A list of contraception methods meeting these criteria is provided in the participant informed consent form.
iv) Diagnosis of Fontan circulation documented in the participant's medical record
Inclusion criteria - Healthy control participants
i) Of full age of consent (at least ≥ 18 years of age) at screening
ii) Signed and dated written informed consent in accordance with ICF-GCP and local regulations prior to admission to the study
iii) Male or female participants
Exclusion criteria - Fontan participants
i) Has previously received a heart or heart-liver transplant
ii) Contraindication for using colesevelam, including allergy
iii) Any physical or mental condition significantly affecting the participant's ability to participate in the investigator's opinion
iv) Women who are pregnant, nursing, or who plan to become pregnant while in the trial
Exclusion criteria - Healthy control participants
i) Any known medical condition
ii) Any physical or mental condition significantly affecting the parti…
What they're measuring
1
Drug safety
Timeframe: 20 Weeks
2
Drug compliance
Timeframe: 20 weeks
3
Impact of colesevelam on plasma & stool bile acid concentration.