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Completed

NCT Number: NCT02889393

Teduglutide for Enterocutaneous Fistula (ECF)

The purpose of this study is to determine whether Teduglutide is safe and feasible to be given for the treatment of enterocutaneous fistula (ECF). The hypothesis is that the drug will be well tolerated and will improve the volume of daily ECF output as well as improve the functional quality of life.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Miami

Miami, Florida, 33136, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18
  • Enterocutaneous fistula (ECF) that could be secondary to volvulus, injury, prior trauma or surgery, or vascular ischemia

Exclusion criteria

  • Perianal fistula
  • Clinical suspicion of inflammatory bowel disease
  • History of radiation enteritis or sprue (as defined by history)
  • Active (<1 year) alcohol or drug abuse
  • Significant hepatic, or cardiac diseases as defined as:
  • Hepatic: aspartate aminotransferase (AST) > 2 times upper limit of normal (10-40 U/L)
  • Cardiac: unstable angina or evidence of active myocardial ischemia (elevated troponin level drawn by clinical suspicion)
  • Severe renal dysfunction: serum creatinine > 2 times upper limit of normal (0.6-1.5 mg/dL)
  • Received glutamine less than 4 weeks prior to screening
  • Receiving growth factors (erythropoietin, granulocyte colony-stimulating factor, granulo-cyte-macrophage colony stimulating factor, and human growth hormone)
  • Pregnancy or lactation (women of childbearing age will be excluded if they do not agree to either complete sexual abstinence during the study or if they refuse to use at least two forms of highly effective contraception such as oral contraception, injectable or implantable contraception, vaginal rings, or intrauterine devices (IUD))
  • Active malignancy or suspicion for gastrointestinal malignancy on CT scan
  • Not capable of understanding or not willing to adhere to the study visit schedule and drug administration requirements
  • Family history of intestinal malignancy (gastric, small intestine, colon)
  • Personal or family history of hereditary non-polyposis colorectal cancer, familial adenomatous polyposis, first degree relative with colon cancer
  • Positive hemoccult (per rectum)
  • Abnormal baseline electrocardiogram (ECF) suggestive of congestive heart failure or underlying cardiac disease
  • Taking oral benzodiazepines, barbiturates, or phenothiazines

Treatment and study plan

Teduglutide

Drug

Daily 0.05 mg/kg Teduglutide administered subcutaneously.

Other names: Gattex

Standard of care

Other

The standard of care treatment of ECF which includes meticulous wound care, optimizations of nutrition, use of acid-suppression medications and anti-motility agents as per treating physician discretion.

Primary outcomes

  1. Change in Average 3-day Fistula Percent Volume

    Time frame: Baseline, Up to 8 weeks

    Percent fistula volume will be reported from the participant

Secondary outcomes

  1. Number of Participants With Ceased Fistula Output

    Time frame: Up to 16 weeks

    As evaluated by treating physician of having at least 1 ceased fistula output

  2. Quality of Life as Measured by ASCQ-Me® v2.0 Social Functioning - Short Form

    Time frame: Up to 16 weeks

    Adult Sickle Cell Quality of Life Measurement (ASCQ-Me) Version 2.0 Social Functioning - Short Form questionnaire has a total score ranging from 5-25 with the higher score indicating a healthier status.

  3. Quality of Life as Measured by the ASCQ-Me® v2.0 Sleep Impact - Short Form

    Time frame: Up to 16 weeks

    Adult Sickle Cell Quality of Life Measurement (ASCQ-Me) Version 2.0 Sleep Impact - Short Form questionnaire has a total score ranging from 5-25 with the higher score indicating a healthier status

  4. Quality of Life as Measured by the PROMIS Scale v1.2 - Global Health

    Time frame: Up to 16 weeks

    Patient Reported Outcome Measures Information Systems Global Health has a total score ranging from 10-50 with the higher score indicating a healthier status

  5. Quality of Life as Measured by the PROMIS Scale v1.0 - Gastrointestinal Belly Pain 5a

    Time frame: Up to 16 weeks

    Patient Reported Outcome Measures Information Systems (PROMIS-GI) Gastrointestinal Belly Pain 5a questionnaire has a total score ranging from 1-25 with the lower score indicating a healthier status

  6. Quality of Life as Measured by the PROMIS Scale v1.0 - Gastrointestinal Diarrhea 6a

    Time frame: Up to 16 weeks

    Patient Reported Outcome Measures Information Systems (PROMIS-GI) Gastrointestinal Diarrhea 6a questionnaire has a total score ranging from 1-30 with the lower score indicating a healthier status

  7. Quality of Life as Measured by the PROMIS Scale v1.0 - Gastrointestinal Nausea and Vomiting 4a

    Time frame: Up to 16 weeks

    Patient Reported Outcome Measures Information Systems (PROMIS-GI) Gastrointestinal Nausea and Vomiting 4a questionnaire has a total score ranging from 1-20 with the lower score indicating a healthier status

  8. Quality of Life as Measured by the PROMIS Scale v2.0 - Ability to Participate in Social Roles and Activities - Short Form 8a

    Time frame: Up to 16 weeks

    Patient Reported Outcome Measures Information Systems (PROMIS) Ability to Participate in Social Roles and Activities - Short Form 8a questionnaire has a total score ranging from 8-40 with the lower score indicating a healthier status

Sponsors and collaborators

Lead sponsor

Daniel Dante Yeh

Other

Collaborators

  • Takeda

Registry information

Official study title

Teduglutide for Treatment of Enterocutaneous Fistula (ECF) - a Pilot Study to Demonstrate Safety and Feasibility

Important dates

Study start
2019
Primary completion
2020
Study completion
2021
First posted
Sep 5, 2016
Registry last updated
Oct 6, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.