In Vivo Optical Spectroscopy Monitoring in a New Model of Muscular Compartment Syndrome
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| ClinicalTrials.gov Identifier: NCT01452425 |
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Recruitment Status :
Completed
First Posted : October 14, 2011
Results First Posted : December 22, 2014
Last Update Posted : December 22, 2014
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Muscular compartment syndrome (MCS) is consecutive to an increase in intramuscular compartment pressures, and is a rare but serious postoperative complication.
The INVOS (In Vivo Optical Spectroscopy) monitors tissular oxygenation continuously and non-invasively.
The objective is to develop a model mimicking the physiopathology of MCS to assess the interest of the INVOS in this case.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Human Volunteers | Device: Tourniquet Device: INVOS assessment Device: EMG assessment | Phase 1 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 10 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Basic Science |
| Official Title: | In Vivo Optical Spectroscopy Monitoring in a New Model of Muscular Compartment Syndrome. |
| Study Start Date : | October 2011 |
| Actual Primary Completion Date : | December 2011 |
| Actual Study Completion Date : | December 2011 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Tourniquet
Inflation of a tourniquet
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Device: Tourniquet
Inflation of a tourniquet (pressure equal to the mean arterial pressure) obtaining a model of slight venous congestion and arterial hypoperfusion Device: INVOS assessment Near Infraread spectroscopy, non invasive Device: EMG assessment Electromyography, non invasive |
- Comparison Between INVOS Monitoring and Electromyography [ Time Frame: 45 minutes ]
A comparison will be made between the INVOS monitoring and non invasive (transcutaneous) EMG monitoring (AP Block), to determine the accuracy of the INVOS monitoring to predict AP block.
Measures were:
[mean (SD)] INVOS (in %) value at baseline and at the time of the block
- Intracompartmental Pressure (ICP) [ Time Frame: 45 minutes ][mean (SD)] ICP (in mmHg), value at baseline and at the time of the block
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| Ages Eligible for Study: | 18 Years to 80 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Healthy volunteers
- >18yr
- Informed consent
- Male
Exclusion Criteria:
- Neuropathies
- Vascular pathology
- Actual pain
- Anti-platelet or anticoagulant therapy
- Ipsilateral history of fracture
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01452425
| Belgium | |
| Cliniques universitaires Saint-Luc | |
| Brussels, Belgium, 1200 | |
| Principal Investigator: | Patrice Forget, M.D. | UCL |
| Responsible Party: | Forget Patrice, MD, Université Catholique de Louvain |
| ClinicalTrials.gov Identifier: | NCT01452425 |
| Other Study ID Numbers: |
B40320107753 |
| First Posted: | October 14, 2011 Key Record Dates |
| Results First Posted: | December 22, 2014 |
| Last Update Posted: | December 22, 2014 |
| Last Verified: | December 2014 |
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Human volunteers |
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Compartment Syndromes Muscular Diseases Musculoskeletal Diseases Vascular Diseases Cardiovascular Diseases |

