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Resuscitation in hostile environments

Randomized controlled clinical trial on basic cardiopulmonary resuscitation and metabolic fatigue in in wilderness environments

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10222040
Enrollment
180
Registered
2019-01-24
Start date
2019-03-01
Completion date
Unknown
Last updated
2024-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic fatigue Nutritional, Metabolic, Endocrine

Interventions

The proposed practical case is the same, a cardiac arrest in which the personnel present in the scene (1 rescuer) must perform the reanimation techniques for 10 minutes until the arrival of the specia

Sponsors

Universidad de Valladolid
Lead Sponsor
Universidad de Castilla la Mancha
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Between 18 and 65 years of age 2. Basic knowledge of basic resuscitation (accredited course or equivalent to the training of AHA or ERC)

Exclusion criteria

Exclusion criteria: 1. Basal heart rate greater than 120 or less than 35 beats per minute. 2. Electrocardiogram with alterations: arrhythmias or changes in the ST segment. 3. Systolic or diastolic blood pressure greater than 160 or 95 mmHg respectively. 4. Systolic blood pressure less than 80 mmHg. 5. Abnormal spirometry (best of three attempts). 6. Oxygen saturation less than 92%. 7. Capillary glycemia below 65 mg / dl. 8. Body mass index greater than 40 Kg / m2. 9. Severe visual or hearing impairment 10. Functional impotence 11. Capillary hemoglobin less than 8 gr. 12. Temperature greater than 38º C. 13. Major surgery 30 days before. 14. Cutaneous diseases in acute phase. 15. Epilepsy. 16. Anticoagulation 17. Infections in progress 18. Systemic immunological diseases.

Design outcomes

Primary

MeasureTime frame
The following are assessed before the participant performs the simulation: 1. Respiratory frequency, assessed using clinical observation 2. Oxygen saturation, assessed using an Masimo Rad 7 3. Heart rate, assessed using a Physio LifePAK® 15 monitor 4. Blood pressure, assessed using a Physio LifePAK® 15 monitor 5. Tympanic temperature assessed using a Braun model ThermoScan® PRO 6000 6. Lactic acid levels, assessed using an Accutrend® Plus meter 7. Blood glucose, assessed using an Accu-Chek® Aviva 8. pH, using saliva strips 9. Hemoglobin level, assessed using an Masimo Rad 7 10. Perfusion index, assessed using an Masimo Rad 7 The following are assessed at the moment the participant performs the simulation every two minutes: 1. Respiratory frequency, assessed using clinical observation 2. Heart rate, assessed using a Physio LifePAK® 15 monitor 3. Lactic acid levels, assessed using an Accutrend® Plus meter 4. pH, using saliva strips 5. Quality level of resuscitation, using the Little Anne QCPR simulator (Laerdal) with QCPR software The following are assessed at the participant performs the simulation, after 10 minutes of rest: 1. Respiratory frequency, assessed using clinical observation 2. Oxygen saturation, assessed using an Masimo Rad 7 3. Heart rate, assessed using a Physio LifePAK® 15 monitor 4. Blood pressure, assessed using a Physio LifePAK® 15 monitor 5. Tympanic temperature assessed using a Braun model ThermoScan® PRO 6000 6. Lactic acid levels, assessed using an Accutrend® Plus meter 7. Blood glucose, assessed using an Accu-Chek® Aviva 8. pH, using saliva strips 9. Hemoglobin level, assessed using an Masimo Rad 7 10. Perfusion index, assessed using an Masimo Rad 7

Secondary

MeasureTime frame
The following are assessed before and after the simulation: 1. Anthropometric study, carried out with the Tanita BC541-N smart scale 2. Anxiety study, through the STAI questionnaire 3. Study of the level of physical activity, using the IPAQ short form questionnaire (this parameter is only evaluated before beginning the study)

Countries

Spain

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026