Last reviewed · How we verify
NCT03952260
Feasibility of 1 Hour Clear Fluid Fasting Prior to Paediatric GA
NA trial testing Fasting time for clear fluid prior to anaesthesia in Gastric Residual Volume in 56 participants. Completed in 15 February 2020.
15 December 2019
Quick facts
| Lead sponsor | Ma Tai Jiun |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | prevention |
| Enrollment | 56 |
| Start date | 15 May 2019 |
| Primary completion | 15 December 2019 |
| Estimated completion | 15 February 2020 |
| Sites | 1 location across Malaysia |
Drugs / interventions tested
- Fasting time for clear fluid prior to anaesthesia
Conditions studied
- Gastric Residual Volume — all drugs for Gastric Residual Volume →
Sponsor
Ma Tai Jiun
Who can join
Adults 5 to 16, any sex, with Gastric Residual Volume. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The study is aim to investigate the appropriate fasting time for clear fluid in paediatric patients who plan for elective minor surgery. This is a randomize control trial, which patient will be selected randomly to fast for clear fluid for 1 hour or 2 hours. It is important to determine the gastric residual volume for paediatric age group prior to elective minor surgery in order to determine whether the difference between 1 hour fasting and 2 hour fasting for clear fluid is significant.
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 NCT03952260
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Gastric Residual Volume
Currently open trials in the same condition.
- NCT07032207 — Correlation of Preoperative Gastric Residual Volume With Body Mass Index and Aspiration Risk in Laparoscopic Bariatric S · 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 NCT03952260 (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 Ma Tai Jiun
- Last refreshed: 2 June 2020
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/NCT03952260.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing