Coma Clinical Trial
Official title:
A Randomised Controlled Study of the Use of Recovery Positions for Comatose Patients in a Resource Limited Setting
Verified date | October 2020 |
Source | University of Oxford |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In resource limited settings, access to one-on-one nursing care and airway protection by intubation may be unavailable. Patients with coma but adequate oxygenation are frequently cared for on medical wards, and nursed by their family members. The investigators previously audited the use of the recovery position in patients with cerebral malaria and found that its usage was greatly increased by an educational intervention aimed at patient's caregivers. A trend to reduction in coma duration and aspiration pneumonia was also found. Since there is no evidence that placing comatose, non-intubated patients in a recovery position improves outcome, the investigators plan to conduct a randomised controlled study comparing standard care with an educational intervention targeting patients' relatives, teaching them to maintain their relative in one of two different recovery positions. With the preliminary efficacy and safety data and feedback that this study will provide, the investigators would then move to conduct a large multicenter study powered to detect a difference in mortality.
Status | Completed |
Enrollment | 1540 |
Est. completion date | March 21, 2020 |
Est. primary completion date | March 21, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Male or female admitted to the medical wards at CMCH - Current GCS < 12 - Less than 5 day history of reduced consciousness - Written informed consent obtained through an adult (=18 years) relative or parent/guardian Exclusion Criteria: - Suspected head or spinal injury/trauma requiring appropriate immobilisation and stabilization - Patient physically restrained by ward staff due to agitation - Unsuitability for lateral positioning e.g. due to burns on lateral aspects, femoral vascular catheter - Requirement for nursing in an upright position e.g. due to respiratory insufficiency - Known or suspected pregnancy - Intubation - Patient or family member previously enrolled in this study. - Consent refused, or no adult (=18 years) relative or parent/guardian present to give consent |
Country | Name | City | State |
---|---|---|---|
Bangladesh | Chittagong Medical College Hospital | Chittagong |
Lead Sponsor | Collaborator |
---|---|
University of Oxford | Chittagong Medical College and Hospital |
Bangladesh,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Composite of aspiration pneumonitis or pneumonia | 48 hours after GCS13 | ||
Secondary | Proportion of patients developing hypoxia | 48 hours after GCS13, | ||
Secondary | Development of pneumonia or pneumonitis, assessed individually | 48 hours after GCS13 | ||
Secondary | Mortality | 7 days post discharge/last follow-up | ||
Secondary | Time to mortality | 7 days post discharge/last follow-up | ||
Secondary | Coma recovery time, defined as time to GCS 15 | during hospitalization (defined as time to GCS 15), expected less than 4 weeks | ||
Secondary | The number of documented episodes of hypoxia | 48 hours after GCS 13 | ||
Secondary | Percentage of observations in the recovery position | whilst GCS<12, expected less than 2 months | ||
Secondary | Modified Rankin scale | on discharge, expected less than 2 months | ||
Secondary | Composite of pressure sore, venous thrombosis, arm or leg peripheral nerve or joint injury | whilst GCS<12, expected less than 2 months | ||
Secondary | Proportion of patients developing a pressure sore | whilst GCS<12, expected less than 2 months | ||
Secondary | Proportion of patients developing a venous thrombosis, | whilst GCS<12, expected less than 2 months | ||
Secondary | Proportion of patients developing a new arm or leg peripheral nerve injury | during hospitalization, expected less than 2 months | ||
Secondary | Proportion of patients developing a new arm or leg joint injury | during hospitalization, expected less than 2 months | ||
Secondary | Trends in Blood presure | measure Systolic and diastolic blood pressure levels | during hospitalization, expected less than 2 months | |
Secondary | Trends in heart rate | during hospitalization, expected less than 2 months | ||
Secondary | Proportion of patients developing peripheral venous cannula function | whilst GCS<12, expected less than 2 months | ||
Secondary | time to hypoxia | 48 hours after GCS13, expected less than 2 months |
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