MatchedQoL: Quality of Life in Patients With Short Bowel Syndrome Treated Without and With Teduglutide - a Prospective Nested Matched Pair Analysis

Sponsor
Charite University, Berlin, Germany (Other)
Overall Status
Recruiting
CT.gov ID
NCT04733066
Collaborator
Takeda (Industry)
40
1
24
1.7

Study Details

Study Description

Brief Summary

The aim of this prospective longitudinal study is to compare the quality of life of short bowel patients prior to and on teduglutide treatment with a non-treated patient group in a matched-pair design.

Condition or Disease Intervention/Treatment Phase

Detailed Description

Short bowel syndrome (SBS) is a malabsorptive disorder mostly caused by surgical interventions, which may result in chronic intestinal failure (cIF). The incidence is progressively increasing due to more aggressive surgical and medical approaches. Parenteral nutrition is still the mainstay of treatment for patients with irreversible cIF. New hormonal therapies hold promise by romoting mucosal growth and intestinal absorption and thereby leading to a consequent reduction in parenteral support and symptoms related to large stomal or faecal losses. Outside the typical primary endpoints of cost data, quality of life (QoL) is an important and yet underappreciated consideration of the effectiveness of targeted therapies. In the clinical STEPS trial, Jeppesen et al. have previously shown a significant improvement of the SBS-QoL total score after 24 week treatment with teduglutide longitudinally but could not identify a statistical significance to the placebo group. Accordingly, Chen and colleagues carried out a post hoc analysis of the afore mentioned clinical trial data based on 86 patients and could confirm the results auf Jeppesen et al. Taken together, these clinical trial data did not show a direct benefit of teduglutide treatment on QoL in these patients, while real life data on QoL changes are not available yet. During the release of teduglutide in Germany, the PNLiver trial (DRKS00010993) recruited chronic intestinal failure patients with parenteral nutrition from 2014 till 2019 to evaluate the capability of non-invasive liver function tests in cIF patients in a cross-sectional (n=90) and longitudinal study (n=20. All participants underwent study visits including clinical examination, dynamic liver function assessment, comprehensive blood tests, nutritional status assessment and quality of life assessment (Short Form 36 [SF-36] and SBS-QoL). Therefore, we have a comprehensive data set of a large monocentric cIF cohort prior to teduglutide treatment. Consequently, our unique QoL data from the PNLiver trail enables a followup assessment for an observation period above 24 weeks of patients who were in the meantime exposed to teduglutide in a real life setting. Nevertheless, QoL also tends to improve with longer duration on HPN. Therefore, we are aiming to extend the results with a pairwise matched control group from non teduglutide-treated PNLiver trail patients and collect follow-up data from this group accordingly.

Study Design

Study Type:
Observational
Anticipated Enrollment :
40 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Quality of Life in Patients With Short Bowel Syndrome Treated Without and With Teduglutide - a Prospective Nested Matched Pair Analysis
Actual Study Start Date :
Sep 1, 2020
Anticipated Primary Completion Date :
Sep 1, 2021
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Non-treatment Group

Quality of life assessment (SBS-QoL, SF- 36) Nutrition status assessment (BIA, BMI) Assessment of functional absorptive small bowel length (citrulline) Clinical data (nutritional program, stool characteristics)

Teduglutide-treated Group

Quality of life assessment (SBS-QoL, SF- 36) Nutrition status assessment (BIA, BMI) Assessment of functional absorptive small bowel length (citrulline) Clinical data (nutritional program, stool characteristics)

Drug: Teduglutide
Intervention group consists of patients, who receive teduglutide within routine medical care

Outcome Measures

Primary Outcome Measures

  1. changes in QoL data during teduglutide therapy [through study completion, an average of 1 year]

    SBS-QoL, SF-36

  2. changes in QoL data of patients without teduglutide therapy [through study completion, an average of 1 year]

    SBS-QoL, SF-36

  3. changes in QoL data of teduglutide treated patients compared to changes in pairwise matched controls [through study completion, an average of 1 year]

    SBS-QoL, SF-36

Secondary Outcome Measures

  1. BMI in kg/m^2 [through study completion, an average of 1 year]

    weight and height will be combined to report BMI in kg/m^2

  2. Body cell mass in kg [through study completion, an average of 1 year]

    measured by bioelectrical impedance analysis

  3. citrulline levels [through study completion, an average of 1 year]

  4. stool characteristics by bristol stool scale [through study completion, an average of 1 year]

    seven types of stool from 1 (hard lumps) till 7 (watery)

  5. parenteral support frequency [through study completion, an average of 1 year]

  6. parenteral support volume [through study completion, an average of 1 year]

  7. parenteral support calories [through study completion, an average of 1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • SBS-associated adult chronic IF with parenteral nutritional support

  • previous inclusion in the PNLiver trial with existing SF-36 and SBSQoL data

  • signed informed consent

Exclusion Criteria:
  • teduglutide stop before study initiation

  • refusal or withdrawal of consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Charite University, Berlin, Germany Berlin Germany 10117

Sponsors and Collaborators

  • Charite University, Berlin, Germany
  • Takeda

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Elisabeth Blüthner, MD, Charite University, Berlin, Germany
ClinicalTrials.gov Identifier:
NCT04733066
Other Study ID Numbers:
  • IIR-DE-002726
First Posted:
Feb 1, 2021
Last Update Posted:
Feb 1, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Elisabeth Blüthner, MD, Charite University, Berlin, Germany
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 1, 2021