ketamine
DrugOne single perfusion of 0.5 mg/kg during 40 minutes at the beginning of the inclusion
NCT Number: NCT02783430
KetaPal is a placebo-controlled randomized trial designed to demonstrate the antidepressant action of ketamine in palliative care situations. Half of participants will receive Ketamine and Milnacipran in combination, while the other half will receive a Placebo and Milnacipran in combination.
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Notify Me18 year and older
All sexes
Interventional
Phase 2 / Phase 3
Chu Amiens Picardie, Amiens, France
Ketamine, a molecule mainly used as an analgesic in palliative care, turns out to be an excellent fast acting antidepressant. By acting as an NMDA receptor antagonist, its mechanism of action is complementary to classical and long acting antidepressants like Selective Serotonin Reuptake Inhibitors (SSRI). In particular, ketamine is able to boost synaptogenesis in only a few hours whereas long-term prescription of SSRI can stimulate neurogenesis.
The purpose of this study is to evaluate a new therapeutic strategy that could integrate ketamine in the same time than SSRI, to control depression symptoms faster and optimize patient's quality of life complementary to treatments of cancer.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
One single perfusion of 0.5 mg/kg during 40 minutes at the beginning of the inclusion
One or two caps per day from the beginning of the inclusion. Milnacipran dosage depending of glomerular filtration rate of patient, during 16 days (doses of 25 or 50 mg or 100mg per day)
One single perfusion during 40 minutes at the beginning of the inclusion
Time frame: At day 1, At day 2
Measure of the change of Depression Intensity
Time frame: at day 0, at day 15
Measure of the improvement of quality of life after 15 days of treatment. EUROHIS-QOL 8-item index, a shortened version of the World Health Organization Quality of Life Instrument-Abbreviated Version (WHOQOL-BREF).
Time frame: at day 0, at day 1, at day 2, at day 4, at day 8, at day 15
measure request of suicidal intentions made by the patient on explicit request of the clinician.
Time frame: at day 0, at day 1, at day 2, at day 4, at day 8, at day 15
The items of the scale limit confounding factors related to physical comorbidity . The answers are simple and quick . It is a wide choice and recommended for depression studies in palliative care.
Time frame: at day 0, at day 4, at day 8, at day 15
The MADRS scale quantifies the intensity of depressive symptoms, determine the number of responders (reduction in the initial score greater than or equal to 50%) and the number of patients in remission (score less than 7).
Time frame: at day 0, at day 1, at day 2, at day 4, at day 8, at day 15
These hetero fast and well validated assessments help to complete the assessment by the clinician on the severity of the patient's situation and overall improvement
Time frame: at day 0, at day 15
Global Assessment of Functioning is a numerical scale ( from 0 to 100) used to evaluate the psychological, social and work of an individual .
Time frame: at day 0, at day 1, at day 2, at day 4, at day 8, at day 15
Symptom Assessment Scale
University Hospital, Lille
Other
Evaluation of the Initial Prescription of Ketamine and Milnacipran Forin Depression in Patients With a Progressive Disease
Acronym: KETAPAL
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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