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NCT03675711: MIDREA
Midline Catheter and Its Impact on Central Lines Removal in ICU
NA trial testing Midline in Vascular Access Device in 83 participants. Terminated before completion.
3 January 2023
Quick facts
| Lead sponsor | Centre Hospitalier Departemental Vendee |
|---|---|
| Phase | NA |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | supportive care |
| Enrollment | 83 |
| Start date | 2 November 2018 |
| Primary completion | 3 January 2023 |
| Estimated completion | 13 January 2023 |
| Sites | 1 location across France |
Drugs / interventions tested
- Midline
- PVC
Conditions studied
- Vascular Access Device — all drugs for Vascular Access Device →
Sponsor
Centre Hospitalier Departemental Vendee
Who can join
18 and older, any sex, with Vascular Access Device. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The study will evaluate 2 strategies to remove central venous catheter (CVC): in one part, the insertion of a midline catheter and in the other part, the conventional insertion of peripheral venous catheter (PVC)
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT03675711
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Midline
Trials testing the same drug.
- NCT06770374 — Effectiveness of a Zinc Oxide Adhesive Securement Device in the Fixation of Midline and Peripherally Inserted Central Ca · NA · recruiting
- NCT03457259 — The Clinical Efficacy of Midline Catheters · NA · completed
Other recruiting trials for Vascular Access Device
Currently open trials in the same condition.
- NCT06604039 — A Clinical Registry to Demonstrate the Safety and Performance of Teleflex Vascular Access Devices · recruiting
Other Centre Hospitalier Departemental Vendee trials
Trials by the same sponsor.
- NCT07489820 — Evaluation of the Efficacy of Negative Pressure Wound Therapy on Perineal Healing Following Abdominoperineal Amputation · NA · not yet recruiting
- NCT07313293 — Impact of Foot Reflexology on Nausea After Obesity Surgery · NA · recruiting
- NCT07314632 — Prospective Study in Laser Treatment of Pilonidal Cysts · recruiting
- NCT07340060 — Statistical Association Between Bicarbonate Levels and Death or Admission to Intensive Care Within 48 Hours in Patients · recruiting
- NCT07228767 — Assessment of Surgeons' Mental Fatigue Based on Operating Time · 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 NCT03675711 (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 Centre Hospitalier Departemental Vendee
- Last refreshed: 22 March 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/NCT03675711.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing