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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04564638
Other study ID # R15518S
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2015
Est. completion date September 1, 2019

Study information

Verified date September 2020
Source Tampere University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

All episodes of patients with acute UC admitted to Tampere University Hospital and treated with intravenous corticosteroids between January 2007 and January 2016 were identified from patient records and reviewed. The risks for colectomy and for continuous use of corticosteroids were evaluated. Predictive factors were analysed.


Description:

Data collected included epidemiological (gender, age at index flare, smoking status), clinical (UC duration, extent of the disease, prior Cs usage, disease severity, laboratory results at index flare) and treatment data (occurrence of new flares, need for further Cs therapy; CyA, thiopurines, biologics or colectomy during follow-up). The diagnosis of UC was made on basis of clinical history, symptoms, endoscopic and histological features. Disease extent was categorized by the Montreal classification and the severity of the flare was assessed by Mayo scoring system based on clinical and endoscopic characteristics. ASUC was characterized by more than six bloody stools/day along with any of the following: tachycardia, elevated temperature, anemia and/or ESR >30 mm/h (Truelove and Witt´s criteria)5. Alleviation of UC was defined as clinical response to intravenous corticosteroids with no need for colectomy or rescue therapy at the same hospitalization as the index flare. Relapse was defined as requiring further corticosteroid treatment, rehospitalization, rescue-therapy, or colectomy later in follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 217
Est. completion date September 1, 2019
Est. primary completion date September 1, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Acute severe ulcerative colitis treated first time with iv corticosteroids

- Follow-up for at least six months after hospitalization or until colectomy.

Exlusion:

-Under 16 year of age

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Corticosteroid


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Tampere University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Colectomy We reviewed patient records for data on need for surgery within follow-up. We identified patients who had emergency colectomy and patients who needed surgery within 1 year of index flare or within follow-up. Long-term follow-up. Years 2007-2016. Mean follow-up of 7.5 years.
Primary Responce to Corticosteroid Responce to first intravenous corticosteroid was defined as no need for colectomy or rescue therapy within admission. Admission on index flare
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