Cancer Pain Clinical Trial
Official title:
Efficacy of Duloxetine in Conjunction With Tramadol for Chronic Cancer Pain
Cancer pain is one of the most common and problematic symptoms. Opioids are typically the most common drugs used in the treatment of cancer pain,they are limited due to their side effects. Tramadol is a centrally acting non-opiate analgesic with low affinity for μ-opioid receptors, and is effective in the treatment of moderate to severe pain. Neuropathic pain is typically not amenable to standard opiate therapy, and the addition of tricyclic antidepressants or/and antiepileptic drugs can offer a very effective treatment strategy in such patients. Duloxetine is a Serotonin Norepinephrine Reuptake Inhibitor (SNRI) that has been used traditionally for its antidepressant qualities and has also analgesic benefit in the treatment of neuropathic pain. Duloxetine exerts its analgesic action through central and peripheral pain modulation .
Status | Not yet recruiting |
Enrollment | 400 |
Est. completion date | December 2023 |
Est. primary completion date | October 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 70 Years |
Eligibility | Inclusion Criteria: - Patients with cancer pain 1. age from 20-70 years old. 2. not receiving any type of analgesia before (opioid naïve, no adjuvants). Exclusion Criteria: 1. Difficult to be assessed for pain. 2. Any contraindication for duloxetine or tramadol. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Assiut University |
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* Note: There are 30 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | concentration of tramadol consumption | all participants(400 patients) will receive tramadol 50 mg twice daily, titration will be done every 3days until 2 weeks,according to changes in visual analogue scale for pain maximum dose will be 400mg daily, one group of participants(200 patients) will receive duloxetine 30mg daily fixed dose in combination with tramadol,decrease in concentration of tramadol consumption means better results,the other group(200 patients) will receive placebo drug once daily in combination with tramadol. | at one month | |
Secondary | concentration of tramadol consumption | all participants(400 patients) will receive tramadol 50 mg twice daily, titration will be done according to changes in visual analogue scale for pain, maximum dose will be 400mg daily, one group of participants(200 patients) will receive duloxetine 30mg daily fixed dose in combination with tramadol,decrease in concentration of tramadol consumption means better results,the other group(200 patients) will receive placebo drug once daily in combination with tramadol. | at 2 month and 3 month | |
Secondary | - change in pain with visual analogue scale | subjective scale by the participants for pain intensity from 0 to 10, minimum value is zero that means no pain, maximum value is 10 that means unbearable pain, higher scores mean worse outcome | at 3,6,9 and 12 days , 2 weeks,1 month,2 month,3 month | |
Secondary | type of pain that relieved better | type of pain that responds better to duloxetine and tramadol (neuropathic or nociceptive), using visual analogue scale for pain intensity (subjective scale by the participants for pain intensity from 0 to 10, minimum value is zero that means no pain, maximum value is 10 that means unbearable pain, higher scores mean worse outcome) | at 1 month,2 month and 3 month | |
Secondary | Leeds Assessment of Neuropathic Symptoms and Signs Scale if neuropathic pain | used for neuropathic pain consists of seven questions minimum value 0 ,maximum value 24,scoring a score of 12 or more suggests pain of predominantly neuropathic origin | at 1 month,2 month and 3 month | |
Secondary | Scale Assessing Pain Intensity and Interference (Pain, Enjoyment, General Activity) | consisting of three questions for the participant,responses from 0 to 10 ,responses to three questions added then divided by three to get a mean score out of ten | at 1 month,2 month and 3 month | |
Secondary | Depression scores by the Patient Health Questionnaire | consists of 9 questions for the participant ,This is calculated by assigning scores of 0, 1, 2, and 3, to the response categories of "not at all," "several days," "more than half the days," and "nearly every day," respectively, total score for the nine items ranges from 0 to 27,higher scores means worse outcome | at 1 month,2 month and 3 month | |
Secondary | Anxiety scores by the Patient Health Questionnaire | consists of 7 questions for the participant ,This is calculated by assigning scores of 0, 1, 2, and 3, to the response categories of "not at all," "several days," "more than half the days," and "nearly every day," respectively, total score for the seven items ranges from 0 to 21,higher scores means worse outcome | at 1 month,2 month and 3 month | |
Secondary | Flanagan Quality of Life Scale | consists of 16 items ,seven responses are delighted(7),pleased(6),mostly satisfied(5),mixed(4),mostly dissatisfied (3),unhappy(2),terrible(1),ranging from 16 to 112,average for healthy 90 | at 1 month,2 month and 3 month | |
Secondary | Side effects as nausea, vomiting, constipation, sedation, arrhythmia and hypertension | participants will be asked about side effects from duloxetine as nausea,vomiting, constipation, sedation, (onset,duration,offset, bearable or not ,affecting quality of life), arrhythmia (type of arrhythmia from electrocardiogram ,onset,duration,offset),hypertension (by measuring blood pressure ,onset ,duration ,offset) | up to 3 month |
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