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NCT05944887
Intravenous Lidocaine to Reduce Propofol Consumption During Gastroscopy.
NA trial testing Lidocaine 2% Injectable Solution in Diagnostic Gastroscopy in 46 participants. Completed in 25 August 2023.
21 August 2023
Quick facts
| Lead sponsor | Erasme University Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | supportive care |
| Enrollment | 46 |
| Start date | 21 July 2023 |
| Primary completion | 21 August 2023 |
| Estimated completion | 25 August 2023 |
| Sites | 1 location across Belgium |
Drugs / interventions tested
- Lidocaine 2% Injectable Solution — full drug profile →
- Saline administration as placebo — full drug profile →
- Propofol injection — full drug profile →
- gastroscopy
Conditions studied
- Diagnostic Gastroscopy — all drugs for Diagnostic Gastroscopy →
Sponsor
Erasme University Hospital
Who can join
Adults 18 to 65, any sex, with Diagnostic Gastroscopy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this clinical trial is to assess if intravenous administration of linisol reduce the propofol consumption and the sides effects of sedation during gastroscopy in healthy patients (ASA 1 and 2 patients). Prior to propofol sedation, participants will receive either an intravenous bolus of linisol (1.5 mg/kg) = treated group or placebo = control group. After the gastroscopy, patients will be asked to complete a satisfaction questionnaire
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 NCT05944887
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Erasme University Hospital trials
Trials by the same sponsor.
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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 NCT05944887 (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 Erasme University Hospital
- Last refreshed: 18 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/NCT05944887.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing