Current partner codePEPTIDESDE
NCT04857801·Not applicable·OBSERVATIONAL

Teduglutide in Short Bowel Syndrome Patients

Status

Completed

Phase

Not applicable

Enrollment

17

Locations

0

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

A retrospective analysis was performed using data of patients suffering from non-malignant SBS-IF. They were treated with teduglutide in a multidisciplinary SBS-IF program at a single university medical center between June 2016 and June 2020.

Interventions

Treatment arms and agents.

DRUG

Teduglutide

effect of teduglutide on intestinal rehabilitation

Timeline

From registration to results.

  1. First posted

    Apr 23, 2021

  2. Study start

    Jun 1, 2016

  3. Primary completion

    Jun 1, 2020

  4. Study completion

    Jun 1, 2020

  5. Results posted

    Not reported

  6. Registry updated

    Apr 26, 2021

Outcomes

What the study measures.

Primary outcomes

enteral autonomy

Time frame · at least 6 months of teduglutide treatment

percentage of patients reaching complete discontinuation of parenteral support

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * SBS-IF Exclusion Criteria: * \< 18 years * Incompliance * \< 6 months of treatment

Study locations

0 registered sites.

No country data reported. Showing up to 24 locations stored in the fast local snapshot.

No study locations reported.

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Teduglutide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.