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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00478569
Other study ID # FP-002-IM
Secondary ID
Status Completed
Phase N/A
First received May 23, 2007
Last updated April 29, 2014
Start date April 2007
Est. completion date March 2013

Study information

Verified date April 2014
Source Takeda
Contact n/a
Is FDA regulated No
Health authority Austria: EthikkommissionDenmark: Ethics CommitteeGermany: Federal Institute for Drugs and Medical DevicesGreece: Ethics CommitteeIreland: Ethics CommitteeNetherlands: N/ASpain: Ethics CommitteeUnited Kingdom: Research Ethics Committee
Study type Observational

Clinical Trial Summary

The primary objective is:

1) to describe adherence (and the main factors influencing adherence) to PTH(1-84) treatment when prescribed in a normal clinical setting.

The secondary objectives are:

1. to describe the demographics and clinical characteristics of the patients that in a normal clinical setting are started on a treatment regimen with PTH(1-84)

2. to describe (using available data) the long term treatment effectiveness during the 24 months following initiation of PTH(1-84) treatment in a normal clinical setting

3. to monitor safety for 24 months following initiation of PTH(1-84) treatment in a patient in a normal clinical setting.


Recruitment information / eligibility

Status Completed
Enrollment 1179
Est. completion date March 2013
Est. primary completion date March 2013
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- According to the current Summary of Product Characteristics (SmPC)

- PTH(1-84) treatment initiated within one month preceding enrolment

- The patient's written informed consent to direct access and data processing must be obtained.

Exclusion Criteria:

- According to the current SmPC

- The patient cannot participate in a clinical trial with PTH (all other trials allowed).

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Drug:
Parathyroid Hormone (PTH) (1-84)
Adherence to PTH(1-84) treatment in Usual Clinical Settings

Locations

Country Name City State
Denmark Nycomed Roskilde

Sponsors (1)

Lead Sponsor Collaborator
Takeda

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants Who Discontinued Before 6 Months of Treatment A participant was defined as "permanently discontinued" if treatment with PTH(1-84) was not ongoing at the 6-month time point and at any future time points afterwards. 6 months No
Secondary Number of Participants Who Discontinued Before 3, 12, 18, and 24 Months of Treatment A participant was defined as "permanently discontinued" if treatment with PTH(1-84) was not ongoing at the 6-month time point and at any future time points afterwards. A participant was defined as "temporarily discontinued" if treatment with PTH(1-84) was not ongoing at the time point but was then ongoing at a future time point. This was the case when a participant or investigator wanted to pause the treatment for a length of time (e.g. because of an adverse event or interruption). Therefore, a participant was defined as still "ongoing" during the trial if treatment with PTH(1-84) had not been permanently or temporarily discontinued at that time point. A participant was only defined as "missing" or "unknown" if they attended the relevant visit and there was no result or "unknown" was entered as the result. Results for months 3, 12, 18 and 24 are cumulative data up until that time point. From enrollment to 3, 12, 18, and 24 months No
Secondary Duration of Treatment Duration of treatment was defined as the last known date that PTH(1-84) was taken minus the first date that PTH(1-84) was taken plus one. In the calculation of duration, no adjustment was made for the prescribed dose frequency or for periods of temporary discontinuation due to adverse drug reactions (ADRs) or temporary patient suspension of treatment. 24 months No
Secondary Treatment Compliance by Visit A participant was defined as compliant if the participant took the treatment as prescribed by the Physician, i.e. complied with the Physician's advice and followed the treatment regimen prescribed. A participant whose dose frequency and treatment length were changed during treatment, e.g. in response to a raised serum calcium level, was regarded as fully compliant if the revised treatment regimen was adhered to.
Data on compliance were obtained at each visit and relate to the period since the previous recorded visit.
From enrollment to 3, 6, 12, 18, and 24 months No