Short Bowel Syndrome
Conditions
Keywords
Liraglutide, Victoza
Brief summary
Pilot study looking at the effect on Liraglutide in the reduction of parenteral support in patients with short bowel.
Interventions
Pilot study of liraglutide in patients with short bowel.
Sponsors
Imperial College London
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Pilot study
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Short bowel (≤200cm) as a result of major intestinal resection (e.g. due to injury, volvulus, vascular disease, Crohn's disease). 2. Jejunostomy patients only 3. 12 continuous months of parenteral support (PS) dependency prior to enrolment. 4. PS required at least 3 times per week to meet their caloric, fluid or electrolyte needs due to on-going malabsorption. 5. Stable PS for at least 4 consecutive weeks immediately prior to first dose of liraglutide. Stability is described as: 1. Actual PS usage should match prescribed PS; 2. Baseline 48-hour urine output is 1-2 L/24 hours. 6. Body mass index ≥ 19.5 kg/m2. 7. Adequate hepatic and renal function: 1. Total bilirubin within the normal range; 2. Alanine aminotransferase (ALT) ≤ 2.5x upper limit of normal; 3. Serum creatinine ≤1.5x upper limit of normal. 8. Stable dosage for \> 4 weeks, prior to baseline evaluations, of anti-motility and anti-diarrhoeal agents, H2 antagonists, proton pump inhibitors, bile sequestering agents and oral rehydration solutions. 9. Female subjects must be on acceptable method of contraception for a minimum of 4 weeks prior to the start of the trial; Acceptable methods of contraception would be a barrier form of contraception, oral contraceptive pill, contraceptive injection or implant or intrauterine implanted device.
Exclusion criteria
* Patients \< 18 years of age * Pregnancy (Female subjects who are not surgically sterile or post menopausal (defined as aged 55 years or older and/or at least 2 years have elapsed since the last menses) or who are not using medically acceptable methods of birth control during and for 30 days after the treatment period. Acceptable methods of contraception would be a barrier form of contraception, oral contraceptive pill, contraceptive injection or implant or intrauterine implanted device. * Active malignancy * Previous malignancy within the past 5 years * History of multiple endocrine neoplasia type 2 (MEN 2) * Personal history or family history of medullary thyroid cancer * Raised serum calcitonin (a biomarker for medullary thyroid cancer) at beginning of trial period * History of cardiac failure * Concurrent use of diuretics * Previous history of pancreatitis * Recent use of other incretin based therapy in the previous 3 months * Concurrent use of octreotide * Type 1 or Type 2 diabetes * Alcohol or drug abuse in last year * \> 4 hospitalisations related to short bowel or its treatment over the previous year * Any hospitalisation 30 days prior to screening * Introduction or dose adjustment of immunosuppressant for inflammatory bowel disease within 6 months, or treatment with biologics within the past 6 months (systemic corticosteroids, methotrexate, cyclosporine, tacrolimus, sirolimus, MMF, infliximab, adalimumab, vedolizumab) * BMI \< 19 kg/m2 or \> 27kg/m2 (An upper cut-off BMI of \> 27kg/m2 has been chosen, as in these patients, there is often a desire to reduce BMI which will conflict with the study design by adding another variable) * Scleroderma/radiation enteritis/coeliacs disease/refractory or tropical sprue * Liver and renal function outside the inclusion range
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Improvement in parenteral support | 20 weeks post start of drug | Improvement of parenteral support on 20 weeks of Liraglutide |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Improvement in quality of life | 20 weeks post start of drug | Improvement in Euroqol EQ5-D score. Level 1: indicating no problem, Level 5: indicating extreme problems. |
| Duration of response | 20 weeks | Duration of response i.e. proportion of subjects who maintain reduction in weekly PN volume from baseline at week 20. |
| Days/Nights not requiring PS | 20 weeks | Days/Nights not requiring PS |
| Change in plasma citrulline, GLP-1, IGF-1 and PYY concentrations | 20 weeks | Change in plasma citrulline, GLP-1, IGF-1 and PYY concentrations |
Countries
United Kingdom
Outcome results
None listed