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| ID | Type | Description | Link |
|---|---|---|---|
| 2007-002415-88 (SLV/EudraCT) | Other Identifier | Statens Legemiddelverk | |
| 911305 (Helse Vest RHF) | Other Identifier | Helse Vest RHF | |
| 82/2007 (P REK Nord) | Other Identifier | Regional Etisk Komite | |
| 16816 (NSD) | Other Identifier | Norsk Samfunnsvitenskapelig Datatjeneste |
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Lack of patients compatible with the protocol´s criteria
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| Name | Class |
|---|---|
| Helse Vest | OTHER |
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Ulcerative colitis is a chronic inflammatory bowel disease caused by an imbalance between natural defence mechanisms in the intestinal mucosa and microbes in the intestinal lumen. We hypothesise that an improvement or even normalisation of this balance may be achieved by the use of vaccines and dietary oats. The combined use of oral typhoid vaccine and cholera/ETEC-vaccine is supposed to stimulate mucosal defence factors, while dietary oats modifies the microbial environment inside the intestinal lumen. Or study aim is to show if such treatment brings symptom relief to patients with ulcerative colitis.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 2 | Experimental | Vaccination with Vivotif and Dukoral |
|
| 3 | Experimental | Dietary supplement with oats |
|
| 4 | Placebo Comparator | Placebo instead of vaccines No dietary supplement |
|
| 1 | Experimental | Vaccination with Vivotif and Dukoral + dietary supplement with oats. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Vaccine Vivotif + Vaccine Dukoral + oats | Biological | Vivotif 1 capsule at study day 1,3,5 and 7. Dukoral oral mixture taken with sodium hydrogen carbonate in water at study day 1 and 14. One daily portion of oats porridge made from oats grain 1dL and water, 6 days a week for 6 months. |
| Measure | Description | Time Frame |
|---|---|---|
| Symptom Score Improvement of 3 or More During or After 6 Months | No patient completed the study, therefore we have no information to report. | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Symptom Score Improvement of 2 or More During or After 6 Months | No patient completed the study, therefore we have no information to report. | 6 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Gunnar Nysæter, MD | Department of Medicine,Haukeland University Hospital, Bergen, Norway | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Medicine, Haukeland Universtiy Hospital | Bergen | 5021 | Norway |
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| ID | Title | Description |
|---|---|---|
| FG000 | Vaccine Arm 2 | Vaccination with Vivotif and Dukoral Vaccine Vivotif + Vaccine Dukoral: Vivotif 1 capsule at study day 1,3,5 and 7. Dukoral oral mixture taken with sodium hydrogen carbonate in water at study day 1 and 14. |
| FG001 | Oats Supplement 3 | Dietary supplement with oats Oats: One daily portion of oats porridge made from oats grain 1dL and water, 6 days a week for 6 months. |
| FG002 | Placebo 4 | Placebo instead of vaccines No dietary supplement Placebo: Placebo capsules instead of Vivotif capsules Placebo mixture instead of liquid Dukoral vaccine |
| FG003 | Vaccine and Oats 1 | Vaccination with Vivotif and Dukoral + dietary supplement with oats. Vaccine Vivotif + Vaccine Dukoral + oats: Vivotif 1 capsule at study day 1,3,5 and 7. Dukoral oral mixture taken with sodium hydrogen carbonate in water at study day 1 and 14. One daily portion of oats porridge made from oats grain 1dL and water, 6 days a week for 6 months. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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|
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| ID | Title | Description |
|---|---|---|
| BG000 | All Arms | Three patients entered the study, one man, two women. Age 24-41 years. The study was terminated due to lack of patients for inclusion. |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Symptom Score Improvement of 3 or More During or After 6 Months | No patient completed the study, therefore we have no information to report. | Posted | 6 months |
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | All Arms | No adverse effects were recorded. |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Gunnar Nysæter or Solomon Tefera or Jan Hatlebakk | Haukeland University Hospital | +47 55972900 | jhat@helse-bergen.no |
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| ID | Term |
|---|---|
| D003093 | Colitis, Ulcerative |
| ID | Term |
|---|---|
| D003092 | Colitis |
| D005759 | Gastroenteritis |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
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| ID | Term |
|---|---|
| C072772 | Ty21a typhoid vaccine |
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|
|
| Vaccine Vivotif + Vaccine Dukoral | Biological | Vivotif 1 capsule at study day 1,3,5 and 7. Dukoral oral mixture taken with sodium hydrogen carbonate in water at study day 1 and 14. |
|
|
| Oats | Dietary Supplement | One daily portion of oats porridge made from oats grain 1dL and water, 6 days a week for 6 months. |
|
| Placebo | Other | Placebo capsules instead of Vivotif capsules Placebo mixture instead of liquid Dukoral vaccine |
|
| Physician Decision |
|
| Participants |
|
| Age, Continuous | Mean | Full Range | years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Secondary | Symptom Score Improvement of 2 or More During or After 6 Months | No patient completed the study, therefore we have no information to report. | Posted | 6 months |
|
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| 0 |
| 3 |
| 0 |
| 3 |
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| D015212 |
| Inflammatory Bowel Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |