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NCT03850041
The Impact of Fluid Volume Shifts on Upper Airway Collapse and Obstructive Sleep Apnea in Surgical Patients
trial in Obstructive Sleep Apnea in 50 participants. Terminated before completion.
14 December 2020
Quick facts
| Lead sponsor | University Health Network, Toronto |
|---|---|
| Status | Terminated |
| Study type | OBSERVATIONAL |
| Enrollment | 50 |
| Start date | 22 July 2019 |
| Primary completion | 14 December 2020 |
| Estimated completion | 14 December 2020 |
| Sites | 2 locations across Canada |
Conditions studied
- Obstructive Sleep Apnea — all drugs for Obstructive Sleep Apnea →
Sponsor
University Health Network, Toronto
Who can join
18 and older, any sex, with Obstructive Sleep Apnea. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The objective of this study is to examine the contribution of intravenous (IV) fluid administration and rostral fluid shift from the legs to the neck thereby leading to worsening of sleep apnea following surgery. In this prospective, observational cohort study, 50 consecutive preoperative adult obstructive sleep apnea (OSA) patients, requiring at least one night hospital stay post surgery, will be recruited. Recent research from general population suggests that intravenous (IV) fluid administration worsens the severity of OSA by shifting of fluid from the legs to the neck thus increasing neck size and causing airway collapse. The results of this study will be used to design future clinical trials evaluating methods to decrease postoperative OSA worsening, as well as decreasing OSA-related postoperative complications.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Perioperative trends in neck and leg fluid volume in surgical patients: a prospective observational proof-of-concept study.
Lukachan GA, Chung F, Yadollahi A, Auckley D, et al · · 2023 · cited 2× · PMID 36450944 · DOI 10.1007/s12630-022-02362-6
Verify or expand the search:
- PubMed search for NCT03850041
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other University Health Network, Toronto trials
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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 NCT03850041 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- 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 Health Network, Toronto
- Last refreshed: 23 June 2022
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/NCT03850041.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing