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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04844788
Other study ID # 08042021
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date April 15, 2021
Est. completion date June 30, 2021

Study information

Verified date April 2021
Source Instituto do Cancer do Estado de São Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

As seen worldwide, cancer incidence is increasing in Latin America achieving an amount of 1.3 million new cases annually.1 In addition, it is expected that up to 70% of patients with cancer will experience pain2, one of the most distressing symptoms in patients with advanced cancer. And despite of advances in cancer therapies, opioids remain the mainstay treatment of cancer-related moderate-to-severe and end-of-life pain.3 However, concerns regarding opioid prescriptions have emerged for reasons like the risk of misuse and the possibility of cancer progression. In the last decades, an increase in consumption of opioids as well as in opioids-related deaths generating the so called 'opioid crisis'. This rise is mainly due to abuse / addiction of opioids. Consequently, oncologic patients are at risk for abuse, as well as for aberrant use, which can complicate the course of cancer treatment.4 5 Another feature of opioids use in cancer patients is that it may contribute to disease progression. Experimental studies suggest that opioids can may lead to immunosuppression and tumor progression or recurrence.6-8 On the other hand, retrospective analysis of clinical data shows conflicting results and trials are lacking.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 20
Est. completion date June 30, 2021
Est. primary completion date May 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria: - Head of anesthesia, Pain management and palliative care departments of cancer hospitals in Latin America. Exclusion Criteria: - Surveys not answered.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Brazil Felipe Porto Rangel Sao Paulo SP

Sponsors (1)

Lead Sponsor Collaborator
Instituto do Cancer do Estado de São Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survey answers answers of the survey sent Up to 3 (three) months
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