AnalgesiaPhase 3INDEXNCT03151863
Intranasal Dexmedetomidine for Procedural Pain Management in Elderly Adults in Palliative Care
A Phase 3 study testing Opioids and Dexmedetomidine in people with Analgesia and Sedation, run by Walid HABRE at 1 site in Switzerland.
Trial summary
Dexmedetomidine is allowed in Switzerland for intravenous (IV) medication in the intensive care unit in the adult patient. Its active molecule, Dexmedetomidine (Dex), is a selective and powerful α2-Adrenoreceptors (AR) agonist that shows the following complementary properties: anxiolytic, sedative and analgesic. Read more about this study
- Who is it for?
- Ages 65 years and older
- Conditions the study is for
- Analgesia, Sedation, Anxiolysis
- What is being tested?
- Opioids and Dexmedetomidine
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 33 participants
- Where
- 1 siteSwitzerland
- Study dates
- 14 Nov 2018to 8 Jun 2021
- Phase
- Phase 3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 65 years and older
- All sexes
- No healthy volunteers
- Older adult
Who may be able to join
- Informed consent signed and dated by the patient or a next of kin;
- ≥65 years old patients;
- Admitted in the palliative medicine unit;
- Undergoing, minimum once per day, a nursing care procedure lasting between 15 and 30 minutes causing discomfort (anxiety, pain or both) and therefore requiring the administration of an extra dose of Morphine, Hydromorphone before the nursing care;
- Taking, on a regularly basis, one of the following opioids: Morphine, Hydromorphone, Buprenorphine, Fentanyl.
Who cannot join
- Known hypersensitivity or allergy to Dexmedetomidine or Midazolam;
- Fentanyl extra dose medication before nursing cares;
- Weight > 80Kg;
- Psychomotor agitation;
- Known bronchial aspiration risks : ileus, vomiting, nausea, clinically relevant gastrooesophageal reflux;
- Known respiratory distress risk: recent need to be ventilated in Intensive Care Unit setting (<7 days), recent change or degradation of the respiratory status (<2 days) with apneas or tachypnea (>20/min), or known sleep apnea without non invasive ventilation; contraindication for nasal drug administration (ex. nasal tumour obstruction);
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- Known cardiac risk : recent cardiac decompensation (<7 days) ; known life threatening or severe heart rate disorders ; bradycardia <60 bpm or known level II or III atrioventricular block without pacemaker ; hypotension with systolic blood pressure less or equal to 100 mmHg; Digoxine treatment;
- Known acute cerebrovascular disease or recent stroke (<1month);
- Already enrolled in another study or previous enrolment into the current study;
- Participation in another study with investigational drug within the 30 days preceding and during the present study.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Intranasal Dexmedetomidine for Procedural Pain Management in Elderly Adults in Palliative Care Setting: a Cross Over, Superiority, Double-blind, Controlled and Randomized Clinical Trial
Dexmedetomidine is allowed in Switzerland for intravenous (IV) medication in the intensive care unit in the adult patient. Its active molecule, Dexmedetomidine (Dex), is a selective and powerful α2-Adrenoreceptors (AR) agonist that shows the following complementary properties: anxiolytic, sedative and analgesic. Moreover, it displays interesting cardiovascular, respiratory and neuropsychic safety and tolerance profiles.
There is increasing number of promising studies for the use of intranasal (IN) Dex in pediatric sedation due to its non-invasive nature, its efficiency and its rare secondary effects. However, there is currently no information in the literature on the use of IN Dex in elderly multi-medicated patients in palliative care.
Read more
In this end-of-life population, pain is controlled with administration of opioids. Procedures, such as nursing cares, can generate pain and anxiety to the patient. Preventive analgesia, subcutaneous (SC) opioids, is administered before the care. However, most of the time, this additional dose fails to relieve the patient from his pain. In SPdol observational study, 42% daily hygiene and comfort nursing care remained painful despite the administration of a preventive analgesia.
IN Dex seems to be a good candidate for non-invasive analgesia and sedation in patients admitted in palliative care before the nursing procedure.
In this study, the investigators compare the efficiency of IN Dex to the regular extradose of SC opioids for analgesia before daily nursing care on elderly patients in the palliative care unit.
The study design is a cross over, two-sided, superiority, double-blind, placebo-controlled and randomized clinical trial.
Read the detailed description
Although necessary for patient wellbeing, nursing care procedures potentially produce discomfort, that should be addressed before the procedures begin. In palliative care setting, daily procedures include mobilisation, hygiene care, wound dressing changes, etc. Non-invasive and simple nursing care procedures may cause anxiety and pain that can lead to a refusal of care or an increased distress. The data on procedural pain prevalence are almost only available in pediatrics and are scarce in palliative care and geriatric population. However, the SPdol french study, conducted on elderly people with palliative situations, showed that 85% of procedural pain was related to daily hygiene and comfort care. Results indicate also that in 42%, this type of care remained painful despite preventive pharmacologic measures as opioids administration. Intensity of procedural pain associated with daily and hygiene care is expected to be moderate to severe and not related to presence or absence of pain before initiation of the procedure but to bad prognostic.
In the context of chronic health problems, comfort management pharmacological interventions to achieve analgesia, slight or conscious sedation during nursing care procedures must ideally combine the following properties:
- Rapid recovery and excellent cardiovascular and respiratory security profile;
- Be administrable in the regular place of care of the patient;
- Minimal requirement for medical surveillance in terms of time, equipment and staff;
- Reproducible inset and outset of the analgesic and anxiolytic effect;
- Easy to titrate;
- Convenient, little or non-invasive and administration route as painless as possible.
Dexmedetomidine is allowed in Switzerland for intravenous (IV) medication in the intensive care unit in the adult patient. It is indicated to obtain a level of sedation no deeper than that allowing a response to a verbal stimulus. Its active molecule, Dexmedetomidine (Dex) is a selective and powerful agonist of α2-adrenoreceptors (AR). This drug has come to be of growing interest in anesthesia and sedation field these last years in literature. Its pharmacological actions on the central nervous system consist in sedative, anesthetic, anxiolytic, analgesic action with good cardiovascular, respiratory and neuropsychic tolerance profile. The main possible secondary effect with IV Dex is bradycardia, due to decreased circulating epinephrine and norepinephrine levels observed with this drug.
Intranasal (IN) administration is an easy-to-use and more efficient alternative than placebo or other sedatives (Midazolam, Ketamine, Chloral) for the sedation of sensitive or less collaborative populations as children and young adults.
IN Dex applications described in the literature include analgesia and sedation for the realization of radiologic investigation, surgical procedures leading to pain and anxiety, dental care, endoscopy and electrochemotherapy, in combination with local anesthesia. IN Dex doses from 1 to 2µg/Kg in young adults and up to 4µg/Kg in children,have been shown to be effective for analgesia and sedation, in these contexts.
From a pharmacological point of view, the superiority of the IN way compared to the oral one has been demonstrated in pediatrics. In healthy adults volunteers IN Dex bioavailability is 82% after a short time (2.6 min on average). The plasmatic peak of concentration is reached after 30 min on average (Tmax range 15-60min). The onset of sedation occurs at 45 min, with a peak effect observed at 90 min.
There is increasing number of promising studies for the use of IN Dex for pediatric sedation due to its non-invasive nature, its efficiency and its rare secondary effects. However, there is currently no information in the literature on the use of IN Dex neither in elderly patients nor in palliative situations.
In end-of-life population, pain is controlled with a subcutaneous administration of opioids as preventive analgesia before nursing cares, when necessary. Most of the time, this supplementary dose fails to relieve the patient from his pain. In SPdol observational study, 42% daily hygiene and comfort nursing care remained painful despite the administration of a preventive analgesia. Opioids limitations to prevent procedural pain are probably linked to anxiety and global discomfort induced by nursing care that opioids alone cannot alleviate. IN Dex seems to be a good candidate for procedural pain comfort pharmacological management giving its analgesic, anxiolytic and sedative properties in old people admitted with palliative situations.
In this study the investigators compare the efficiency of IN Dex to the regular additional dose of opioids for analgesia, sedation and anxiolysis for daily nursing care on end-of-life elderly patients.
The population of interest is widely heterogeneous according to its disease and medication. Moreover the pain feeling is specific to each person. Therefore a cross-over design was chosen so the patient is his own control. Each patient participates to 2 nursing care procedures where he receives both SC and IN administration. However, each time only one treatment is active while the other one is a placebo. Ex : SC placebo and IN Dex.
After a period of wash-out (24 to 48h), the patient receives , on the next nursing care procedure, the complementary treatment combination (ex: SC opioids and IN placebo).
To minimize bias, randomization is done by the pharmacy, on the treatment sequence and the study is double-blinded. In case of inefficient analgesia, the patient receives a rescue dose of Dormicum, 0.05mg/Kg.
During each procedure the patient is monitored with validated tools for pain, anxiety, sedation, heart rate and oxygen saturation.
The sedation state of the patient is assessed up to 45 minutes after treatment administration. At 45 minutes, the peak effect of the drugs (opioids as well as Dex) is reached and the nursing care can start and lasts for 15 to 30 minutes. The patient is followed-up during two hours after the end of the care. The total procedure lasts for 3h30 total.
- Conditions
- Analgesia, Sedation, Anxiolysis
- Being tested
- Opioids, Dexmedetomidine, Placebo
- Keywords
- Dexmedetomidine, Opioids, Palliative Care, Elderly people, Nursing care, Analgesia, Sedation, Anxiolysis, Intranasal
- Medical subject headings
- Agnosia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
OpioidsDrug
Also called Opioid prescribed to the patient on routine basis
The usual opioid treatment used for nursing care
DexmedetomidineDrug
Also called Dexdor
Dexmedetomidine is provided intranasally
PlaceboDrug
Also called Normal saline
Normal saline is either given subcutaneously or intranasally
| Study group | Role | What they receive |
|---|---|---|
| Opioids, placebo | Active comparator | One single dose of subcutaneous opioids and intranasal placebo (NaCl0.9%). Receives: Drug: Opioids; Drug: Placebo |
| Placebo, Dexmedetomidine | Experimental | One single dose of subcutaneous placebo (NaCl0.9%) and intranasal Dexmedetomidine 1.25ug/Kg Receives: Drug: Dexmedetomidine; Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Total score for ECPA over 5
To assess the pain of the patient, a nurse will use the ECPA scale (Elderly Pain Caring Assessment). This is a validated tool to assess pain and anxiety intensity with 8 items based on the behaviour of the non-communicating elder person. The scale is divided in two: the first part is used for the pain assessment before the care while the second part assesses the pain during the care.
The minimum score is 0. The maximum score is 32. One to five minutes are needed to do the evaluation depending on the experience of the observer.
The pain is assessed 5 minutes before the care and then continuously during the care. When the total score between "before" and "during the care" exceeds 5, the patient is considered as having pain.
Measured: Minutes 35
Secondary outcomes (4)
Time to reach a level of sedation of mOAA less or equal to 4 before the care
The modified Observer's Assessment of Alertness/Sedation Scale (mOAA/S) is a validated tool with 7 levels, easy and rapid to use. One minute is sufficient to complete the assessment. The sedation state is evaluated every 15 minutes between the time when the drug is administered and the start of the care.
Measured: Minutes 45
Time to come back to the initial sedation state
The initial sedation state is evaluated with the mOAA/S scale before the administration of the drugs. After the end of the care, the sedation state of the patient is assessed every 30 minutes until he reaches his initial sedation state within maximum 2h.
Measured: Hour 2
anxiety
The anxiety (yes/no) is assessed with the ECPA scale. This scale includes anxiety items and will be used for this purpose also (see outcome 1).
Measured: Minutes 35
Pain evolution
The pain is assessed by the patient himself using a Visual Analogue Scale
Measured: Minutes 90
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 May 2017
- Study start14 Nov 2018
- Primary completion8 Jun 2021
- Study completion8 Jun 2021
Why it stopped: Lack of budget
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for AnalgesiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- This two-sided, superiority, cross-over trial is based on a clinically relevant reduction (≥20%) of primary outcome (ECPA pain score \>5) with the Dexmedetomidine treatment versus standard active control (opioids). It requires a sample size of 52 patients for a paired analysis with an intra-patient correlation of 50%. Type I error: 0.05 and type II error: 0.20. 25% of drop-out are expected. In consequence, 66 patients are required for the study.
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 33 participants (actual)
Sponsor and investigators
- Lead sponsor
- Walid HABRE
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Walid HABRE, University Hospital, Geneva
- Investigators
- Walid Habre, MD, PhD, Study director, University of Geneva, Switzerland
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03151863
- Sponsor's protocol ID
- INDEX_NDR
- Acronym
- INDEX
- Status last verified
- Jul 2021
- First submitted
- 31 Mar 2017
- Last updated
- 28 Jul 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: In case of request for a systematic review/meta-analysis, IPD can be shared after publication.
Publications
Dieudonne Rahm N, Zaccaria I, Gil Wey B, Pautex S, Habre W, Elia N. Intranasal Dexmedetomidine for Pain Management in Older Patients: A Cross-Over, Randomized, Double-Blinded, Active-Controlled Trial. Drugs Aging. 2023 Jun;40(6):527-538. doi: 10.1007/s40266-023-01027-3. Epub 2023 May 11.
PubMed 37170043
Study at a glance
From the registry record, last updated by the sponsor on 28 Jul 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Intranasal Dexmedetomidine for Procedural Pain Management in Elderly Adults in Palliative Care Setting: a Cross Over, Superiority, Double-blind, Controlled and Randomized Clinical Trial
- ClinicalTrials.gov ID
- NCT03151863
- Acronym / sponsor ID
- INDEX / INDEX_NDR
- Conditions
- Analgesia, Sedation, Anxiolysis
- Keywords
- Dexmedetomidine, Opioids, Palliative Care, Elderly people, Nursing care, Analgesia, Sedation, Anxiolysis
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Lack of budget
- Enrolment
- 33 participants (actual)
- Lead sponsor
- Walid HABREUniversity, hospital or other
- Study start
- 14 Nov 2018 (actual)
- Primary completion
- 8 Jun 2021 (actual)
- Study completion
- 8 Jun 2021 (actual)
- First posted
- 12 May 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Dexmedetomidine is allowed in Switzerland for intravenous (IV) medication in the intensive care unit in the adult patient. Its active molecule, Dexmedetomidine (Dex), is a selective and powerful α2-Adrenoreceptors (AR) agonist that shows the following complementary properties: anxiolytic, sedative and analgesic. Moreover, it displays interesting cardiovascular, respiratory and neuropsychic safety and tolerance profiles.
There is increasing number of promising studies for the use of intranasal (IN) Dex in pediatric sedation due to its non-invasive nature, its efficiency and its rare secondary effects. However, there is currently no information in the literature on the use of IN Dex in elderly multi-medicated patients in palliative care.
In this end-of-life population, pain is controlled with administration of opioids. Procedures, such as nursing cares, can generate pain and anxiety to the patient. Preventive analgesia, subcutaneous (SC) opioids, is administered before the care. However, most of the time, this additional dose fails to relieve the patient from his pain. In SPdol observational study, 42% daily hygiene and comfort nursing care remained painful despite the administration of a preventive analgesia.
IN Dex seems to be a good candidate for non-invasive analgesia and sedation in patients admitted in palliative care before the nursing procedure.
In this study, the investigators compare the efficiency of IN Dex to the regular extradose of SC opioids for analgesia before daily nursing care on elderly patients in the palliative care unit.
The study design is a cross over, two-sided, superiority, double-blind, placebo-controlled and randomized clinical trial.
Detailed description
Although necessary for patient wellbeing, nursing care procedures potentially produce discomfort, that should be addressed before the procedures begin. In palliative care setting, daily procedures include mobilisation, hygiene care, wound dressing changes, etc. Non-invasive and simple nursing care procedures may cause anxiety and pain that can lead to a refusal of care or an increased distress. The data on procedural pain prevalence are almost only available in pediatrics and are scarce in palliative care and geriatric population. However, the SPdol french study, conducted on elderly people with palliative situations, showed that 85% of procedural pain was related to daily hygiene and comfort care. Results indicate also that in 42%, this type of care remained painful despite preventive pharmacologic measures as opioids administration. Intensity of procedural pain associated with daily and hygiene care is expected to be moderate to severe and not related to presence or absence of pain before initiation of the procedure but to bad prognostic.
In the context of chronic health problems, comfort management pharmacological interventions to achieve analgesia, slight or conscious sedation during nursing care procedures must ideally combine the following properties:
- Rapid recovery and excellent cardiovascular and respiratory security profile;
- Be administrable in the regular place of care of the patient;
- Minimal requirement for medical surveillance in terms of time, equipment and staff;
- Reproducible inset and outset of the analgesic and anxiolytic effect;
- Easy to titrate;
- Convenient, little or non-invasive and administration route as painless as possible.
Dexmedetomidine is allowed in Switzerland for intravenous (IV) medication in the intensive care unit in the adult patient. It is indicated to obtain a level of sedation no deeper than that allowing a response to a verbal stimulus. Its active molecule, Dexmedetomidine (Dex) is a selective and powerful agonist of α2-adrenoreceptors (AR). This drug has come to be of growing interest in anesthesia and sedation field these last years in literature. Its pharmacological actions on the central nervous system consist in sedative, anesthetic, anxiolytic, analgesic action with good cardiovascular, respiratory and neuropsychic tolerance profile. The main possible secondary effect with IV Dex is bradycardia, due to decreased circulating epinephrine and norepinephrine levels observed with this drug.
Intranasal (IN) administration is an easy-to-use and more efficient alternative than placebo or other sedatives (Midazolam, Ketamine, Chloral) for the sedation of sensitive or less collaborative populations as children and young adults.
IN Dex applications described in the literature include analgesia and sedation for the realization of radiologic investigation, surgical procedures leading to pain and anxiety, dental care, endoscopy and electrochemotherapy, in combination with local anesthesia. IN Dex doses from 1 to 2µg/Kg in young adults and up to 4µg/Kg in children,have been shown to be effective for analgesia and sedation, in these contexts.
From a pharmacological point of view, the superiority of the IN way compared to the oral one has been demonstrated in pediatrics. In healthy adults volunteers IN Dex bioavailability is 82% after a short time (2.6 min on average). The plasmatic peak of concentration is reached after 30 min on average (Tmax range 15-60min). The onset of sedation occurs at 45 min, with a peak effect observed at 90 min.
There is increasing number of promising studies for the use of IN Dex for pediatric sedation due to its non-invasive nature, its efficiency and its rare secondary effects. However, there is currently no information in the literature on the use of IN Dex neither in elderly patients nor in palliative situations.
In end-of-life population, pain is controlled with a subcutaneous administration of opioids as preventive analgesia before nursing cares, when necessary. Most of the time, this supplementary dose fails to relieve the patient from his pain. In SPdol observational study, 42% daily hygiene and comfort nursing care remained painful despite the administration of a preventive analgesia. Opioids limitations to prevent procedural pain are probably linked to anxiety and global discomfort induced by nursing care that opioids alone cannot alleviate. IN Dex seems to be a good candidate for procedural pain comfort pharmacological management giving its analgesic, anxiolytic and sedative properties in old people admitted with palliative situations.
In this study the investigators compare the efficiency of IN Dex to the regular additional dose of opioids for analgesia, sedation and anxiolysis for daily nursing care on end-of-life elderly patients.
The population of interest is widely heterogeneous according to its disease and medication. Moreover the pain feeling is specific to each person. Therefore a cross-over design was chosen so the patient is his own control. Each patient participates to 2 nursing care procedures where he receives both SC and IN administration. However, each time only one treatment is active while the other one is a placebo. Ex : SC placebo and IN Dex.
After a period of wash-out (24 to 48h), the patient receives , on the next nursing care procedure, the complementary treatment combination (ex: SC opioids and IN placebo).
To minimize bias, randomization is done by the pharmacy, on the treatment sequence and the study is double-blinded. In case of inefficient analgesia, the patient receives a rescue dose of Dormicum, 0.05mg/Kg.
During each procedure the patient is monitored with validated tools for pain, anxiety, sedation, heart rate and oxygen saturation.
The sedation state of the patient is assessed up to 45 minutes after treatment administration. At 45 minutes, the peak effect of the drugs (opioids as well as Dex) is reached and the nursing care can start and lasts for 15 to 30 minutes. The patient is followed-up during two hours after the end of the care. The total procedure lasts for 3h30 total.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
- Model description
- This two-sided, superiority, cross-over trial is based on a clinically relevant reduction (≥20%) of primary outcome (ECPA pain score >5) with the Dexmedetomidine treatment versus standard active control (opioids). It requires a sample size of 52 patients for a paired analysis with an intra-patient correlation of 50%. Type I error: 0.05 and type II error: 0.20. 25% of drop-out are expected. In consequence, 66 patients are required for the study.
| Arm | Type | Receives |
|---|---|---|
| Opioids, placebo | Active comparator | Drug: Opioids, Drug: PlaceboOne single dose of subcutaneous opioids and intranasal placebo (NaCl0.9%). |
| Placebo, Dexmedetomidine | Experimental | Drug: Dexmedetomidine, Drug: PlaceboOne single dose of subcutaneous placebo (NaCl0.9%) and intranasal Dexmedetomidine 1.25ug/Kg |
Who may qualify
- Ages
- 65 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Older adult
Key inclusion criteria (5 listed)
- Informed consent signed and dated by the patient or a next of kin;
- ≥65 years old patients;
- Admitted in the palliative medicine unit;
- Undergoing, minimum once per day, a nursing care procedure lasting between 15 and 30 minutes causing discomfort (anxiety, pain or both) and therefore requiring the administration of an extra dose of Morphine, Hydromorphone before the nursing care;
- Taking, on a regularly basis, one of the following opioids: Morphine, Hydromorphone, Buprenorphine, Fentanyl.
Key exclusion criteria (10 listed)
- Known hypersensitivity or allergy to Dexmedetomidine or Midazolam;
- Fentanyl extra dose medication before nursing cares;
- Weight > 80Kg;
- Psychomotor agitation;
- Known bronchial aspiration risks : ileus, vomiting, nausea, clinically relevant gastrooesophageal reflux;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| OpioidsAlso: Opioid prescribed to the patient on routine basisThe usual opioid treatment used for nursing care | Drug | Opioids, placebo |
| DexmedetomidineAlso: DexdorDexmedetomidine is provided intranasally | Drug | Placebo, Dexmedetomidine |
| PlaceboAlso: Normal salineNormal saline is either given subcutaneously or intranasally | Drug | Opioids, placebo, Placebo, Dexmedetomidine |
Primary outcome
Total score for ECPA over 5
Time frame: Minutes 35
To assess the pain of the patient, a nurse will use the ECPA scale (Elderly Pain Caring Assessment). This is a validated tool to assess pain and anxiety intensity with 8 items based on the behaviour of the non-communicating elder person. The scale is divided in two: the first part is used for the pain assessment before the care while the second part assesses the pain during the care. The minimum score is 0. The maximum score is 32. One to five minutes are needed to do the evaluation depending on the experience of the observer. The pain is assessed 5 minutes before the care and then continuously during the care. When the total score between "before" and "during the care" exceeds 5, the patient is considered as having pain.
4 secondary outcomes
Time to reach a level of sedation of mOAA less or equal to 4 before the care
Time frame: Minutes 45
Time to come back to the initial sedation state
Time frame: Hour 2
anxiety
Time frame: Minutes 35
Pain evolution
Time frame: Minutes 90
Results and safety
The study was stopped early (reason given: Lack of budget). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Jul 2021.
- Derived from this study: PubMed 37170043Dieudonne Rahm N, Zaccaria I, Gil Wey B, Pautex S, Habre W, Elia N. Intranasal Dexmedetomidine for Pain Management in Older Patients: A Cross-Over, Randomized, Double-Blinded, Active-Controlled Trial. Drugs Aging. 2023 Jun;40(6):527-538. doi: 10.1007/s40266-023-01027-3. Epub 2023 May 11.
- Individual participant dataSharing planned: Undecided. In case of request for a systematic review/meta-analysis, IPD can be shared after publication.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Walid Habre, MD, PhD study director
University of Geneva, Switzerland
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Opioids and Dexmedetomidine in people with Analgesia and Sedation, run by Walid HABRE at 1 site in Switzerland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 28 Jul 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: Lack of budget). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Total score for ECPA over 5 (time frame: Minutes 35). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03151863, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jul 2021.