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Treatment with Tapentadol in Cancer Patients

Not Applicable
Conditions
Health Condition 1: G893- Neoplasm related pain (acute) (chronic)
Registration Number
CTRI/2020/11/029206
Lead Sponsor
Manipal Academy of Higher Education
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients of age >18 years and <70 years, from either sex.

Patients with moderate to severe pain {pain >4 measured on numerical rating scale (NRS)}.

Willing to participate in the study and provide written informed consent.

Exclusion Criteria

Pregnant/lactating women.

Patients already on MAO inhibitors, serotonin reuptake inhibitors, and Tricyclic antidepressants [contraindicated drugs].

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
A treatment algorithm for Tapentadol therapy for pain management in palliative cancer patientsTimepoint: 3 years
Secondary Outcome Measures
NameTimeMethod
Pharmacogenomic profile and Population Pharmacokinetic model of TapentadolTimepoint: 3 years
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