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Crohns DiseaseEUSNCT01582568

EUS Evaluation of Perianal and Peri-rectal Fistulizing Crohn's Disease With CERTOLIZUMAB Treatment

An observational study of Crohns Disease, run by Baylor College of Medicine at 1 site in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

The primary objective of this study is to assess perianal and perirectal fistula healing (complete closure) based on endoscopic ultrasound (EUS) evaluation at 3 months and by PDAI (Pouchitis Disease Activity Index) and Fistula Drainage assessment by 6 months, showing no fistula (new or recurrence) in treatment of… Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Crohns Disease
What is being tested?
Certolizumab
Type of treatment
Injection or infusion
How many people
1 participants
Where
1 siteUnited States
Study dates
Jun 2011to Mar 2014
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Crohn's disease patients with peri-anal or peri-rectal fistulizing disease. Moderate to severe Crohn's disease patients between the ages of 18 and 70 years with active peri-anal or peri-rectal fistula.

Who may be able to join

  • Conventional therapy here indicates non-biologic therapy. Study subjects would have failed conventional and standard regimens of treatment such as immunomodulators (azathioprine, 6-mercaptopurine, methotrexate) or mesalamines or corticosteroids. Certolizumab is actually an approved regimen of treatment for Crohn's disease as patients with perianal fistulas fall under those with moderately to severely active disease. It is not an off-label indication, therefore would not require an IND. The study goal is to look at EUS as a tool to determine how fistula healing occurs with the use of certolizumab which is one of the biologic therapies used to treat fistulizing Crohn's disease. Crohn's disease patients with peri-anal or peri-rectal fistulizing disease. Moderate to severe Crohn's disease patients between the ages of 18 and 70 years with active peri-anal or peri-rectal fistula.

Who cannot join

  • Pre-existing fistula improving on current medical therapy. Contraindication to certolizumab use. Prior use of anti-TNF-alpha.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Baylor College of Medicine

    Houston, Texas, 77030

Other trials in United States

About this study

The primary objective of this study is to assess perianal and perirectal fistula healing (complete closure) based on endoscopic ultrasound (EUS) evaluation at 3 months and by PDAI (Pouchitis Disease Activity Index) and Fistula Drainage assessment by 6 months, showing no fistula (new or recurrence) in treatment of Crohn's' disease patient with Certolizumab (Cimzia).

Read the detailed description

Peri-anal ( located around the anus, the opening of the rectum to the outside of the body) fistulae are a major complication of Crohn's disease and occur in almost 30% of patients. Patients with perianal fistulae suffer from severe pain, perianal drainage, and have significant impairment of quality of life. Initial studies of Infliximab and Adalimumab in patients with CD have shown perianal fistula healing with these medications. Infliximab and Adalimumab are medications which reduce the effects of a substance in the body that can cause inflammation. They are also used to treat Crohn's disease after other drugs have been tried without successful treatment of symptoms. Although no studies have specifically evaluated Certolizumab (Cimzia) treatment in fistulizing Crohn's disease, there is evidence to its efficacy. Certolizumab reduces the effects of a substance in the body that can cause inflammation. Certolizumab is used to treat the symptoms of Crohn's disease after other drugs have been tried without successful treatment of symptoms. Studies with a small number of patients who use Cimzia did not show any significant effect on fistula closure. However, in a larger subgroup of patients with fistulae in PRECiSE 2 43.3% of those who received 3 induction injections of certolizumab followed by placebo, and 53.6% of those on certolizumab 400mg continuous treatment had fistula closure defined as no drainage on gentle compression of at least 50% of open fistulae at any 2 consecutive visits, at least 3 weeks apart. Perianal disease activity is usually monitored clinically. In clinical studies, two evaluation methods have been used in attempts to unify the definition of perianal disease activity. One method is the perianal Crohn's disease activity index (PDAI) which involves questions regarding discharge, pain/ restriction of activities, restriction of sexual activity, type of perianal disease, degree of induration (with scores >/=5 indicating active disease, with decrease in PDAI of 2 or more points indicates improvement, and consider 0 as healed. PDAI scale (Pouchitis Disease Activity Index). This scale analyzes and summarizes different criteria: clinical, endoscopic and histological. Among clinical symptoms, an important factor is the number of stools exceeding the post-operative average, bleeding, re-occuring stomachaches, as well as body temperature above 37.8°C or 100°F. "Pouchitis" is a term to describe inflammatory changes in the pouch created from the lower part of the ileum. The patients suffer from high body temperature, stomachaches and watery stools with small amounts of mucus, blood and soiling. An exam based technique, used in the Precise trials is the Fistula Drainage Assessment indicating improvement or remission with closure of individual fistulae defined as no fistula drainage despite gentle finger compression, improvement defined as a decrease from baseline in the number of open draining fistulae of greater than or equal to 50 percent for at least 2 consecutive visits (i.e. at least 4 weeks), and remission defined as closure of all fistulae that were draining at baseline for at least 2 consecutive visits (i.e., at least 4 weeks). However both have not been validated, and the response levels are usually evaluated several months into treatment. If another method could provide early assessment / predictors of healing, it could make the decision for the treatment of the gastroenterologist as well as the patient, easier to determine if they should continue the biologic or stop. Studies have evaluated the use of endoscopic ultrasound (EUS) to follow fistula assessment and healing, but none have specifically assessed this in response to certolizumab treatment. EUS is increasingly used and has been found to be equally accurate in the evaluation of perianal fistulae compared to MRI of the pelvis. An accurate assessment and classification of fistulae can facilitate further management including surgical planning, further medical treatment, or a combination of both. EUS can evaluate for fistulae as well as abscesses and the relation to the anatomic landmarks of the rectum including the sphincter muscles as well as adjacent organs such as vagina and the bladder. EUS has the advantage of being more convenient for the patient than an MRI. An MRI can take a long duration, can cause anxiety in those that are claustrophobic, and is expensive. EUS is usually performed with sedation and by the treating physician allowing a more personal evaluation of the fistula anatomy and correlation of endoscopic mucosal findings. Thus, we propose to evaluate the use of certolizumab in Crohn's disease patients with peri-anal and peri-rectal fistulae (an abnormal passage that leads from an abscess or hollow organ or part to the body surface or from one hollow organ or part to another) and to assess their response and healing (A perirectal abscess is a collection of pus in the deep tissues surrounding the anus. Perirectal and perianal abscesses are thought to develop from the glands surrounding the anus) based on EUS findings. This study can help provide recommendations on fistula classification of EUS and use this classification to provide EUS - based early predictors of response of treatment with certolizumab.

Conditions
Crohns Disease
Being tested
Certolizumab
Medical subject headings
Crohn Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CertolizumabDrug

    Also called Cimzia

    Certolizumab 200mg-400mg subcutaneous every 2 weeks for 8 weeks.

Study groups in NCT01582568
Study groupRoleWhat they receive
CertolizumabSubjects will take the study drug certolizumab for 8 weeks. They will undergo a endoscopy before study drug and then again after study is complete. The study doctor will be looking for complete closure of the peri-anal fistula identified at visit 1 after the use of certolizumab based on and endoscopic ultrasound (EUS).
Receives: Drug: Certolizumab

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The response rate

    The primary objective of this study is to assess perianal and perirectal fistula healing (complete closure) based on endoscopic ultrasound (EUS) evaluation at 3 months and by PDAI (Pouchitis Disease Activity Index) and Fistula Drainage assessment by 6 months, showing no fistula (new or recurrence) on treatment of Certolizumab (Cimzia) in Crohn's's disease patient s.

    Measured: 6 months

Secondary outcomes (1)
  1. Fistula healing based on EUS

    The secondary objectives: 1. To define an Endoscopic Ultrasound (EUS)-based classification system which will compare and analyze perianal and perirectal fistulizing (abnormal opening between two hollow organs) in Crohn's disease. 2. To compare the EUS classification to PDAI and Fistula Drainage Assessment scores. 3. To determine EUS-based early predictors which can be summarized by the findings/results of the EUS procedure of fistula healing with Certolizumab (Cimzia) treatment.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Apr 2012 (estimated)
  2. Study startJun 2011
  3. Primary completionMar 2014
  4. Study completionMar 2014

Why it stopped: Not enough subjects to reach accrual goals.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01582568
Sponsor's protocol ID
H-26958
Acronym
EUS
Status last verified
Feb 2016
First submitted
19 Apr 2012
Last updated
19 Feb 2016
Results posted
No
Data monitoring committee
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Crohns Disease, run by Baylor College of Medicine at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 19 Feb 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Not enough subjects to reach accrual goals.). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The response rate (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Feb 2016; AzTrials last refreshed its copy on 8 Nov 2026.

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