Clinical trial · Observational
Our Anesthesia Experience During MRI Scan
NCT03123302CI-TRIAL-00045413completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In this study we aim to investigate the relationship between our anesthesia practice and post procedure complications after MRI scanning with sedation. This is a retrospective, single center observational study. All patients undergoing MRI scan during the study period will be included.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Epileptic Seizure | — | UNRESOLVED | — |
| Intracranial Aneurysm | — | UNRESOLVED | — |
| Intracranial Hypertension | — | UNRESOLVED | — |
| Intracranial Tumor | Intracranial Neoplasm | ALIAS | 0.90 |
| Vertebra; Anomaly | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (4)
- label
- Group 1
- description
- Epileptic patients who are sedated with a total dose of propofol 2 mg/kg and midazolam 0.1 mg/kg.
- label
- Group 2
- description
- Epileptic patients who are sedated with a total dose of pentothal 4 mg/kg and midazolam 0.1 mg/kg.
- label
- Group 3
- description
- Non-epileptic patients who are sedated with a total dose of propofol 1 mg/kg and ketamine 1 mg/kg.
- label
- Group 4
- description
- Non-epileptic patients who are sedated with a total dose of midazolame 0.1 mg/kg and ketamine 1 mg/kg.
Primary outcomes (1)
- measure
- Patient characteristics anesthesia choice and possible complications during MRI anesthesia.
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria:All patients undergoing MRI scan wth sedation anesthesia and giving written informed consent. Exclusion Criteria: patients refusal to be studied. \-
References
Publications (0)
Data not yet available
No reference posted for this study.