AzTrials
AzTrials

SpondyloarthritisNCT04369651

Socio-economic Determinants for Acceptance and Choice of Biological Treatment

An observational study of Spondyloarthritis, run by National Center for Rheumatic Diseases, Nepal.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This was a cross-sectional study conducted at National center for rheumatic diseases, Nepal on SpA patient refractory to initial treatment with conventional anti rheumatic drugs. Patients taking TNFi (tumor necrosis factor inhibitor- adalimumab or etanercept) or tofacitinib were included. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Spondyloarthritis
How many people
117 participants
Where
No sites listed yet
Study dates
1 Jun 2015to 31 Dec 2019
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with SpA and enrolled in the cohort database from June 2015 to December 2019 were selected.

Who may be able to join

  • patients with spondyloarthropathy
  • on any oral or injectable forms of biological treatment

Who cannot join

  • less than 18years of age
  • who did not consent for participation
  • deferred from biological treatment due to comorbid conditions like concurrent infections or heart failure

About this study

Official title: Socio-economic Determinants for Acceptance and Choice of Biological Treatment by Patients With Spondyloarthropathy in Nepal

This was a cross-sectional study conducted at National center for rheumatic diseases, Nepal on SpA patient refractory to initial treatment with conventional anti rheumatic drugs. Patients taking TNFi (tumor necrosis factor inhibitor- adalimumab or etanercept) or tofacitinib were included. Baseline demographic, socio-economic, clinical data were recorded.

Read the detailed description

This was a cross-sectional observational study conducted in the rheumatology clinic of National Center for Rheumatic Diseases, Kathmandu, Nepal. Patients with spondyloarthropathy (SpA) and enrolled in the cohort database from June 2015 to December 2019 were selected. Those taking any oral or injectable forms of biological treatment were included in the study. Patients less than 18 years of age, who did not consent for participation or additional information, who were deferred from biological treatment due to comorbid conditions like concurrent infections or heart failure were excluded. An informed consent was obtained from selected patients and any additional information required was taken via e-mail or telephone enquiry.

Diagnostic \& measurement tools Diagnosis of SpA was made by rheumatologists on the basis of the modified New York Criteria for Ankylosing Spondylitis and the ASAS criteria (Assessment of SpondyloArthritis International Society) for axial and peripheral SpA. Diagnosis of nr-axial SpA was made by MRI evidence of sacroilitis in a patient with normal radiograph with or without HLA B27. Disease activity was assessed using composite Ankylosing Spondylitis Disease Activity Score (ASDAS) and the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI).

Socioeconomic status Socioeconomic factors studied were educational level and the primary occupation. Patient self-reported highest educational level was recorded and was categorized into illiterate, primary, secondary, higher secondary, above secondary level education. Occupation and social class were recorded based on self-report primary source of income. It was categorized into homemakers, students, service holders, business, teachers, farmers and others (field workers, labor workers). A dedicated research officer also took data on other demographic parameters and geographical location of residence. Geographical location was categorized into urban-rural and hilly-plain terrain.

Indications for offering biological treatment Indications for biological or small molecule treatment included: a. Failure of at least 2 courses of NSAIDS, b. Failure of at least 3months of conventional synthetic DMARDs (csDMARDs). For patients with PsA, the csDMARDs included methotrexate and/or leflunomide; for AS, nr-axial SpA and IBD-associated arthritis, it included sulfasalazine and/or methotrexate. Failure of treatment was defined as: a. Persistent ASDAS of ≥2.1, b. Improvement of ASDAS by less than -1.1, c. Persistent BASDAI of ≥4. All patients fulfilling these indications were offered biological treatment. Patients with no contraindication for TNFi were offered either injectable biologicals (adalimumab or etanercept: only TNFi available in Nepal) or tofacitinib (only small molecule available in Nepal) and explained about the preparatory investigations, dosage of TNFi, storage, cost, monitoring and side-effects.

Data collection and analysis Complete data on baseline demographic parameters (age, gender, address, education, occupation) and ASDAS and BASDAI scores at initiation of treatment with biological or small molecule were recorded in a hardcopy data-sheet and later entered to a predesigned excel-sheet by a trained research officer.

Statistical analysis was performed using SPSS version 21 (IBM Corp, USA). Simple descriptive statistics were used to analyze various socioeconomic and demographic parameters. Chi-squared test was used to analyze difference in these parameters between patients who chose injectable and those who chose tofacitinib. Linear regression analysis was performed to identify variables associated with use of any biological agent. All variables with p-value of <0.05 were analyzed in multiple regression model to evaluate the independent association. Difference in mean values between two treatment groups were assessed by independent t-test.

Keywords
socio-economic determinants, biologic, Nepal, low income country, spondyloarthroathy
Medical subject headings
Spondylarthritis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. socio economic determinants

    socio economic determinants for acceptance of biologic therapy

    Measured: four years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Apr 2020
  2. Study start1 Jun 2015
  3. Primary completion31 Dec 2019
  4. Study completion31 Dec 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
117 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04369651
Sponsor's protocol ID
210/2017
Status last verified
Apr 2020
First submitted
28 Apr 2020
Last updated
1 May 2020
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Spondyloarthritis, run by National Center for Rheumatic Diseases, Nepal.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 May 2020. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

socio economic determinants (time frame: four years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 May 2020.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in