Anesthesia Clinical Trial
— DEPTHipOfficial title:
A Multicenter Randomized Controlled Trial in Elderly Patients With Hip Fractures Comparing Continuous Fascia Iliaca Compartment Block to Systemic Opioids and Its Effect on Delirium Occurrence
Verified date | August 2023 |
Source | Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A broken hip occurs frequently in elderly patients and is often very painful. Side effects of inadequately treated pain as well as the traditional drugs (administered through intravenous catheter) used to treat pain are, among others, a confusional state, called delirium. When pain medication is administered locally, only around the hip joint, pain might be treated more effectively and these side effects could be prevented. This is called a nerve block. The current study evaluates the use of a continuous nerve block throughout the complete hospital admission with a catheter around the hip joint versus the use of traditionally used pain medication administered though an intravenous catheter in elderly patients with a broken hip. Half of all patients will receive the nerve block while in the emergency department and the other half will receive pain medication through the intravenous access.
Status | Terminated |
Enrollment | 239 |
Est. completion date | July 19, 2023 |
Est. primary completion date | July 19, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 55 Years and older |
Eligibility | Inclusion Criteria: - adult patients aged = 55 years with - a radiographically confirmed hip fracture Exclusion Criteria: - multiple injuries (polytrauma patients) - previous adverse reaction or known allergy to local anaesthetics or opioids or paracetamol - skin infection in proximity of injection site - delirious state at presentation in the ED |
Country | Name | City | State |
---|---|---|---|
Netherlands | Meander Medical Center | Amersfoort | |
Netherlands | Academic Medical Center | Amsterdam | |
Netherlands | Slotervaart Medical Center | Amsterdam | |
Netherlands | VU Medical Center | Amsterdam | |
Netherlands | Tergooi Ziekenhuis | Hilversum | Noord Holland |
Lead Sponsor | Collaborator |
---|---|
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) | ZonMw: The Netherlands Organisation for Health Research and Development |
Netherlands,
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* Note: There are 22 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | occurrence of delirium | Diagnosis will be based on DSM-IV criteria. During hospital admission screening is actively. After discharge, information is gathered by contacting patients and family members, general practitioners or nursing facilities | three months | |
Secondary | duration of delirium | duration is defined as the total number of days with delirium. | three months | |
Secondary | severity of delirium | severity is defined as percentage of patients with delirium duration > 2 days. | three months | |
Secondary | NRS pain scores | NRS pain scores during complete hospital stay, NRS pain scores will be recorded in the Emergency Department before the intervention as well as after the intervention at 30-minutes time intervals (this is according standard protocol in case opioids are administered). During hospital stay, during each nursing shift, a minimum of one NRS pain score is documented. | from hospital admission until 48 hours after surgery | |
Secondary | need for additional analgesia | need for rescue analgesia will be documented during complete Emergency Department and hospital stay. | hospital admission until 48 hours after surgery | |
Secondary | patient satisfaction | satisfaction of patients and health care staff regarding efficacy of pain treatment and method of pain treatment is recorded in the Emergency Department and daily during hospital admission (5-point Likert scales and reference questions). | from hospital admission until 48 hours after surgery | |
Secondary | length of hospital stay | defined as total consecutive days admitted in the hospital. | from hospital admission until discharge; an average of 9 days | |
Secondary | ICU admission | binary endpoint, whether patient is admitted to the ICU at any moment during hospital stay. | from hospital admission until discharge; an average of 9 days | |
Secondary | ICU length of stay | defined as total days admitted to the ICU department. | from hospital admission until discharge; an average of 9 days | |
Secondary | hospital re-admission rate | a re-admission occurs when a patient is admitted to the hospital within three months after initial discharge (from hip fracture related admission). | three months | |
Secondary | medical complications | all events regarding infections, renal- or pulmonary function and cardiovascular events will be accounted for. | three months | |
Secondary | surgical complications | defined as dislocations and fractures. | three months | |
Secondary | mortality | all cause in-hospital-mortality and mortality after hospital discharge. | three months | |
Secondary | activities of daily living | 15-item modified Katz Index of Activities of Daily Living at three months after discharge. Baseline will be 2 weeks before presentation. | three months | |
Secondary | generic quality of life | generic HRQol (Euroqol - EQ-5D-5L) at three months after discharge. Baseline will be 2 weeks before presentation. | three months | |
Secondary | Oxford hip score | Oxford Hip Score after 3 months. | three months | |
Secondary | cognitive function with Mini Mental State Examination | Mini Mental State Examination at inclusion in the study, at hospital discharge and at three months after discharge. | three months | |
Secondary | cost effectiveness analysis | primary focus on direct medical costs, direct non-medical costs, indirect costs and productivity loss. | three months |
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