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Study identifier: NCT07439692 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingICOPE

ICU-related Out of Pocket Expenses (ICOPE)

Condition: Cost of ICU · Out of Pocket Expenses  ·  Sponsor: Nat Intensive Care Surveillance - MORU

PhaseN/A
Planned participants354
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where44 locations · 12 countries

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The ICU-related Out-of-Pocket Expenses (ICOPE) study is a multinational, prospective observational study conducted in African and Asian countries to quantify ICU-related out-of-pocket expenditures and catastrophic health expenditure among patients and families. The study will include all patients admitted to participating ICUs during a predefined 14-day recruitment window, provided they have an ICU stay longer than 24 hours and informed consent is obtained. A minimum sample size of 354 patients is planned, including both ventilated and non-ventilated patients. Participants will be followed until ICU discharge, with additional follow-up at 30 days and 6 months after admission, resulting in a total study duration of 18 months. The primary objective is to quantify ICU-related out-of-pocket costs and assess the proportion of patients experiencing catastrophic health expenditure, comparing ventilated and non-ventilated groups, while secondary objectives include identifying risk factors for catastrophic expenditure and documenting coping strategies used by families to manage ICU costs.

This description comes directly from the study's public registry record.

Talk to the study team

Dr  ·  +393291525693  ·  luigipisani@gmail.com

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: All patients admitted to the participating ICUs during a predefined window of 14 days and expected to have a duration of stay \>24 hours will be eligible for the study. Exclusion Criteria: lack informed consent.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (44)

Wazir Akbar Khan HospitalKabul, Kabul, AfghanistanRecruiting
Ibne-e-Sina Emergency HospitalKabul, Kabul, AfghanistanRecruiting
Sheikh Zayed HospitalKabul, Kabul, AfghanistanRecruiting
Rabia Balkhi HospitalKabul, Kabul, AfghanistanRecruiting
Apollo Imperial HospitalChittagong, Chattogram Division, BangladeshRecruiting
Chattogram Medical College HospitalChittagong, Chattogram Division, BangladeshRecruiting
CSCRChittagong, Chattogram Division, BangladeshRecruiting
250 Bedded General HospitalChittagong, Chittagong, BangladeshRecruiting
Bangladesh Institute of Applied Health Sciences (BIAHS)Dhaka, Dhaka Division, BangladeshRecruiting
Komfo Anokye Teaching Hospital (KATH)Kumasi, Ashanti Region, GhanaRecruiting
JSS Medical College, MysoreMysore, Karnataka, IndiaRecruiting
Amrita Institute of Medical SciencesKochi, Kerala, IndiaRecruiting

+ 32 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

KabulChittagongDhakaKumasi

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