Mirtazapine in Cancer-related Poly-symptomatology

Cancer Clinical Trial

— MIR-P  

Official title:

What is the Effectiveness and Safety of Mirtazapine Versus Escitalopram in Alleviating Cancer-associated Poly-symptomatology (MIR-P)? A Mixed-method Randomized Controlled Trial Protocol

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04763135
• Other study ID #: 69HCL20_0032
• Secondary ID: 2020-002994-90
• Status: Terminated
• Phase: Phase 3
• Start date: December 15, 2021
• Est. completion date: December 17, 2021

Study information

• Verified date: June 2023
• Source: Hospices Civils de Lyon
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Multicenter, prospective, randomized, controlled trial based on a mixed-method methodology using parallel groups, of oral mirtazapine (intervention) compared with oral escitalopram (control), with a 56 days follow-up. Improvement of the Global health Status (issued from the EORTC-QLQ-C30 (Quality of Life Questionnaire)) will be used as the primary outcome on day 56. Semi-structures interviews will be performed on a purposive sample for qualitative analysis. The 418 participants will be followed-up at day 7, 14, 28 and 56 for a 56 days period. A sub-group of participants will be invited to take part into qualitative interviews at baseline and day 56. Recruitment of participants to the qualitative part will be based on a purposive sampling.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 1
• Est. completion date: December 17, 2021
• Est. primary completion date: December 17, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Being over 18 years old
• Suffering from advanced cancer
• Having a clinically estimated life expectancy over 3 months.
• Being diagnosed from having a depressive syndrome by a Hospital Anxiety and Depression Scale-D over 11.
• Being in need of an antidepressant treatment.
• Suffering from at least one under-controlled symptom (defined as a score over 3 on the Edmonton Symptom Assessment Scale) among: pain, nausea, vomiting, breathlessness, lack of appetite, sleep disorders, anxiety or impaired wellbeing.
• Having or not a cancer treatment.
• Being able to understand the information related to the study, and to sign informed consent.
• Having agreed to take part to the study.
• Being able to fill Patient Reported Outcomes questionnaires.
• Being available to be call on days 7 and 14.
• Having a social security affiliation.

Exclusion Criteria:

• Being treated by an antidepressive agent during the four weeks before inclusion.
• Having had a hypersensitivity event to mirtazapine, escitalopram of any excipient.
• Having had a prior inefficient treatment by mirtazapine or escitalopram.
• Having postural hypotension or arterial systolic hypotension inferior to 90 mmHg measured following the guidelines of the European Society of Cardiology
• Having a QT interval over 420 ms.
• Having uncontrolled hearth rhythm disorder or uncontrolled conduction disorder.
• Having had or having bipolar disorder.
• Having uncontrolled seizure or epilepsy (relative non-inclusion criteria needing a neurology specialist opinion)
• Having or having history of closed-angle glaucoma.
• Having bone marrow aplasia.
• Practicing breast-feeding or being pregnant.
• Women of childbearing age with no contraception method.
• Having a treatment with:
• Monoamine oxidase inhibitors (Selegiline, Moclobemide, Isocarboxazid, Nialamide, Phenelzine, Tranylcypromine, Iproniazid, Iproclozide, Toloxatone, Linezolid, Safinamide, Rasagiline)
• One of the following antiarrhythmic drugs: Flecainide, Propafenone, any class IA and III antiarrhythmic drug (amiodarone, disopyramide, hydroquinidine, quinidine, procainamide, sparteine, ajmaline, prajmaline, lorajmine, bretylium tosilate, bunaftine, dofetilide, ibutilide, tedisamil, dronedarone).
• Linezolid, sparfloxacin, moxifloxacin, macrolides (IV erythromycin, josamycin, clarithromycin, telithromycin), pentamidin, halofantrine, HIV protease inhibitors (ritonavir, nelfinavir, amprenavir, indinavir), azolic antifungal agents (ketoconazole, itraconazole, miconazole, fluconazole, voriconazole)
• Mizolastine and Astémizole
• St. John's wort
• Having genetic galactose intolerance or glucose-galactose malabsorption.
• Having one of the following electrolyte disorders not corrected at the time of inclusion: hyponatremia, hyperkalemia, hypokalemia, hypermagnesemia, and hypomagnesemia.
• Having end-stage renal disease with a creatinine clearance inferior to 15 ml/min calculated using the Cockroft's formula.
• Having hepatic failure.
• Having legal incapacity

Related Conditions & MeSH terms

• Cancer
• Neoplasm Metastasis
• Neoplasms

Intervention

Drug:
• Mirtazapine
Orally disintegrating tablets of mirtazapine introduced at the dose of 15 mg and increased up to 45 mg per day during 56 days. Doses escalation: based on symptom management and side effect assessment.
• Escitalopram
Orally disintegrating tablets of escitalopram introduced at the dose of 10 mg (or 5 mg for patients older than 65) and increased up to 20 mg per day during 56 days. Doses escalation: based on symptom management and side effect assessment.

Locations

Country	Name	City	State
France	Centre Hospitalier Universitaire de Clermont-Ferrand	Cébazat
France	Centre Hospitalier Universitaire de Grenoble	La Tronche
France	Centre Léon Bérard	Lyon
France	Centre Médico-Chirurgical de Réadaptation des Massues Croix-Rouge française	Lyon
France	Hôpital de la Croix-Rousse	Lyon
France	Hôpital Edouard Herriot	Lyon
France	Institut Curie	Paris
France	Centre Hospitalier Lyon Sud	Pierre-Bénite
France	Centre Hospitalier Universitaire de Saint-Etienne	Saint-Étienne
France	Hôpitaux universitaires de Strasbourg	Strasbourg
France	Centre Hospitalier de Valence	Valence

Sponsors (1)

Lead Sponsor	Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Global health status score	The Global Health Status will be calculated from the specific subscale included in the EORTC-QLQ-C30 scale.; The difference between baseline and the end-point (day 56) will be the primary judgment criteria. A 4 to 8 points difference between baseline and endpoint will be considered as a mild difference, and a difference over 8 points will be considered as a moderate difference.	At baseline and day 56
Secondary	The subjective experience associated with symptoms burden.	Qualitative analysis of compared semi-structured interviews undertaken at baseline and day 56 on a convenience sample.	At baseline and day 56.
Secondary	Proportion of mitigated symptoms.	The Edmonton Symptom Assessment Scale 12F will be used to assess each symptoms intensities for the following symptoms: pain, nausea, vomiting, lack of appetite, breathlessness, depression, anxiety, sleep disorders and wellness.; For each symptom, the difference between baseline and the assessment time will be calculated. A difference equal or over one point will be regarded as mitigation. The judgment criteria will be the proportion of symptoms that were rated over three at baseline and that were mitigated at the assessment time.	Day 28
Secondary	Proportion of mitigated symptoms.	The Edmonton Symptom Assessment Scale 12F will be used to assess each symptoms intensities for the following symptoms: pain, nausea, vomiting, lack of appetite, breathlessness, depression, anxiety, sleep disorders and wellness.; For each symptom, the difference between baseline and the assessment time will be calculated. A difference equal or over one point will be regarded as mitigation. The judgment criteria will be the proportion of symptoms that were rated over three at baseline and that were mitigated at the assessment time.	Day 56
Secondary	Auto-assessment depression score.	The Hospital Anxiety and Depression Scale-D auto-assessment score will be used to assess the auto-assessment depression score.; The judgment criteria will be the difference between baseline and the assessment time. A difference over 1.5 points will be regarded as clinically significant.	Day 28
Secondary	Auto-assessment depression score.	The Hospital Anxiety and Depression Scale-D auto-assessment score will be used to assess the auto-assessment depression score.; The judgment criteria will be the difference between baseline and the assessment time. A difference over 1.5 points will be regarded as clinically significant.	Day 56
Secondary	Hetero-assessment-based depression score.	The Montgomery-Asberg Depression Rating Scale hetero-assessment score will be used to assess the hetero-assessment depression score.; The judgment criteria will be the difference between baseline and the assessment time. A difference over 1.9 points will be regarded as clinically significant.	Day 28
Secondary	Hetero-assessment-based depression score.	The Montgomery-Asberg Depression Rating Scale hetero-assessment score will be used to assess the hetero-assessment depression score.; The judgment criteria will be the difference between baseline and the assessment time. A difference over 1.9 points will be regarded as clinically significant.	Day 56
Secondary	Weight control	Weight control will be defined as a difference under 500g between the weight at baseline minus the weight at the assessment time.; The judgment criteria will be the proportion of patients with weight control at assessment time.	Day 28
Secondary	Weight control	Weight control will be defined as a difference under 500g between the weight at baseline minus the weight at the assessment time.; The judgment criteria will be the proportion of patients with weight control at assessment time.	Day 56
Secondary	Weight improvement.	Weight improvement will be defined as a difference over 500g between the weight at the assessment time minus the weight at baseline.; The judgment criteria will be the proportion of patients with weight improvement at assessment time.	Day 28
Secondary	Weight improvement.	Weight improvement will be defined as a difference over 500g between the weight at the assessment time minus the weight at baseline.; The judgment criteria will be the proportion of patients with weight improvement at assessment time.	Day 56
Secondary	Stability in oral morphine milligram equivalents.	The stability in oral morphine milligrams equivalent will be defined as a decrease or stability in the daily doses of opioid pain killers measured using oral morphine milligram equivalents.; The judgment criteria will be the proportion of patients with stability in oral morphine milligram equivalents.	Day 28
Secondary	Stability in oral morphine milligram equivalents.	The stability in oral morphine milligrams equivalent will be defined as a decrease or stability in the daily doses of opioid pain killers measured using oral morphine milligram equivalents.; The judgment criteria will be the proportion of patients with stability in oral morphine milligram equivalents.	Day 56
Secondary	Escalation in symptom control treatment doses	Escalation in symptom control treatment doses will be defined as any escalation in the dose of a treatment existing at baseline or any new treatment introduced to control one of the following symptoms: pain, nausea, vomiting, lack of appetite, breathlessness, depression, anxiety, sleep disorders and wellness.; The judgment criteria will be the proportion of patients with an escalation in symptom control treatment doses.	Day 28
Secondary	Escalation in symptom control treatment doses	Escalation in symptom control treatment doses will be defined as any escalation in the dose of a treatment existing at baseline or any new treatment introduced to control one of the following symptoms: pain, nausea, vomiting, lack of appetite, breathlessness, depression, anxiety, sleep disorders and wellness.; The judgment criteria will be the proportion of patients with an escalation in symptom control treatment doses.	Day 56
Secondary	Number of side effects.	The number of side effects will be used to assess the security of use. It will be assessed using the Antidepressant Side Effect Checklist and side effects will be considered if rated moderate or severe.	Day 7
Secondary	Number of side effects.	The number of side effects will be used to assess the security of use. It will be assessed using the Antidepressant Side Effect Checklist and side effects will be considered if rated moderate or severe.	Day 14
Secondary	Number of side effects.	The number of side effects will be used to assess the security of use. It will be assessed using the Antidepressant Side Effect Checklist and side effects will be considered if rated moderate or severe.	Day 28
Secondary	Number of side effects.	The number of side effects will be used to assess the security of use. It will be assessed using the Antidepressant Side Effect Checklist and side effects will be considered if rated moderate or severe.	Day 56
Secondary	Medication adherence.	The medication adherence will be assessed using the Medication Adherence Rating Scale score at day 56 and the Proportion of Days Covered all along the follow-up period.	Day 56
Secondary	Symptoms' intensities auto-assessment on the following symptoms: pain, nausea, vomiting, lack of appetite, breathlessness, depression, anxiety, sleep disorders and wellness.	The Edmonton Symptom Assessment Scale 12F will be used to assess each symptoms intensities for the following symptoms: pain, nausea, vomiting, lack of appetite, breathlessness, depression, anxiety, sleep disorders and wellness.; For each symptom, the difference between baseline and the assessment time will be used as the judgment criteria. A difference equal or over one point will be regarded as clinically significant.	Day 28
Secondary	Symptoms' intensities auto-assessment on the following symptoms: pain, nausea, vomiting, lack of appetite, breathlessness, depression, anxiety, sleep disorders and wellness.	The Edmonton Symptom Assessment Scale 12F will be used to assess each symptoms intensities for the following symptoms: pain, nausea, vomiting, lack of appetite, breathlessness, depression, anxiety, sleep disorders and wellness.; For each symptom, the difference between baseline and the assessment time will be used as the judgment criteria. A difference equal or over one point will be regarded as clinically significant.	Day 56