View Clinical Trial (Medical Research Study)
Endoscopic Ultrasound (EUS) Guided Treatment With Humira for Crohn's Perianal Fistulas - NCT00517296-37232(Clinical Trial 180455)
ClinicalConnection.com has recently undergone an update and this page may no longer be up-to-date. Please Search For Clinical Trials to view the most current clinical trials listings.
| City: |
|
Nashville |
|
State:
|
|
TN |
| Zip Code: |
|
37232 |
| Conditions: |
|
Crohn Disease - Rectal Fistula |
| Purpose: |
|
This study is to assess whether utilizing endoscopic ultrasound(EUS) to guide treatment can
improve durable fistula healing in patients with Crohn's perianal fistulas and to get
preliminary information regarding the effectiveness of Adalimumab for Crohn's perianal
fistulas.
|
| Study summary: |
|
|
| Criteria: |
|
Inclusion Criteria:
A patient may be considered for study participation if all of the following apply:
- Male and Female aged 18 years or older; and
- A confirmed diagnosis of Crohn's disease and one or more identifiable perianal
fistulas.
Exclusion Criteria:
A patient will be excluded from the study if one or more of the following apply:
- Females who are pregnant or breast feeding;
- Infliximab received within 6 weeks prior to study entry;
- Patients who cannot take, or refuse to take concomitant immunosuppressive therapy
with either azathioprine, 6-mercaptopurine, or methotrexate; Unless patient has been
intolerant of these therapies in the past or is contraindicated as determined by the
investigator;
- Patients who cannot take, or refuse to take concomitant antibiotic therapy;
- Patients with severe anal stenosis or tenderness which would preclude colonoscopy and
/ or rectal EUS;
- Patients who cannot take or refuse to take adalimumab;
- Patients with active or latent tuberculosis;
- Patients who have had systemic antibiotic, antiviral or antifungal treatment(s)
within 3 weeks prior to Screening for all non-Crohn's related infections;
- Patients concurrently taking anakinra (Kineret);
- Patients with a history of cancer or lymphoproliferative disease other than a
successfully and completely treated cutaneous squamous cell or basal cell carcinoma
or carcinoma in-situ of the cervix;
- Patients with chronic hematologic problems such as bleeding dyscrasias;
- Patients with a history of demyelinating disease (i.e. multiple sclerosis); and
- Patients with congestive heart failure. |
|
|
|
|
|
|
|
|
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
|
| Trials Alerts: |
|
If you would like to be
notified of new clinical trials as they become available please
register for a free account.
|
|
| Data Source: |
|
ClinicalTrials.gov |
| Date Processed: |
|
June 11, 2010 |
Modifications to
this listing: |
|
Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
|
|
|
|
|
|
|
|