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Recruiting NCT07357558

A Qualitative Study Investigating the Lived Experiences and Impact of Reproductive Issues in Adults With Primary Ciliary Dyskinesia

Observational Primary Ciliary Dyskinesia (PCD)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Interview only.
Who it may be relevant to
Registry conditions: Primary Ciliary Dyskinesia (PCD). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United Kingdom
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Study involving undertaking research interviews with adults who have primary ciliary dyskinesia in the UK about their views and experiences of fertility, pregnancy and parenthood

Interventions

  • Other Interview only
    No intervention

Primary outcome measures

  • Qualitative description of views and experiences of participants [Time frame: Explored during study interview (day 1)]

Eligibility criteria

Inclusion criteria

  • Lives in United Kingdom
  • 'likely' or 'confirmed' diagnosis of PCD
  • able and willing to sign the consent form

Exclusion criteria

  • unwilling to participate in the study
  • not meeting inclusion criteria

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

United Kingdom · 1 center
  • University Hospitals Southampton NHS Trust — Southampton

Identifiers

NCT: NCT07357558 · RHM O&G0332

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗