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NCT06028607: (PCD)
Feasibility of Consumption of Nutritional Supplementation in Primary Ciliary Dyskinesia
NA trial testing QD-27 in Primary Ciliary Dyskinesia in 15 participants. Completed in 28 February 2022.
29 November 2021
Quick facts
| Lead sponsor | University of Leeds |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | other |
| Enrollment | 15 |
| Start date | 17 May 2021 |
| Primary completion | 29 November 2021 |
| Estimated completion | 28 February 2022 |
| Sites | 1 location across United Kingdom |
Drugs / interventions tested
- QD-27
Conditions studied
- Primary Ciliary Dyskinesia — all drugs for Primary Ciliary Dyskinesia →
Sponsor
University of Leeds
Who can join
17 and older, any sex, with Primary Ciliary Dyskinesia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Feasibility study to understand and gain preliminary information on tolerability and palatability of an oral nutritional supplement gel in a clinical Primary Ciliary Dyskinesia population. To determine if dietary intake is affected by the consumption of the nutritional supplement. Explore possible future outcome measures that could be important in determining impact of this nutritional intervention on this patient group. Participants will be provided with the gel supplements and alongside will have other standard and non standard care measures assessed lung function (FEV1%) number of exacerbation's during study period vitamin D status Bio impedance analysis (BIA) skin-fold measures (e.g. Tricep Skin-fold (TSF) Mid upper arm circumference (MUAC) Handgrip strength (HGS) quality of life measures 6-minute walking tests. Hypothesis Patients with PCD can successfully consume 2 gel supplements per day for a period of 3 months with no effect on dietary intake.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06028607
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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- NCT05685186 — A Longitudinal, Observational Study of Primary Ciliary Dyskinesia in Adults · active not recruiting
- NCT04602481 — Living With Primary Ciliary Dyskinesia (Living With PCD) · recruiting
Other University of Leeds trials
Trials by the same sponsor.
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- NCT07181915 — Changing Outcomes Through Achievement Emails in COPD Using Routine Healthcare Audits · NA · active not recruiting
- NCT06240403 — Digoxin and Senolysis in Heart Failure and Diabetes Mellitus · Phase 2 · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06028607 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Leeds
- Last refreshed: 13 September 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06028607.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing