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Breakthrough Cancer Pain clinical trials

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NCT ID: NCT05531422 Completed - Clinical trials for Breakthrough Cancer Pain

Effectiveness and Tolerance of Inhaled Fentanyl Aerosol (25µg/Dose) in Chinese Patients With BTcP

Start date: October 20, 2021
Phase: Phase 2
Study type: Interventional

Breakthrough cancer pain (BTcP) is a common problem in patients with cancer. This is a phase IIa dose-response and safety study of inhaled fentanyl aerosol (25µg/dose) in Chinese patients with breakthrough cancer pain.

NCT ID: NCT03895762 Completed - Clinical trials for Breakthrough Cancer Pain

Observational Study of Efficacy, Safety and Tolerability of Fentanyl in Korean Cancer Patients

OASIS
Start date: July 4, 2017
Phase:
Study type: Observational

The purpose of this observational study is: To observe the efficacy, safety, and tolerability of Abstral ODT for the alleviation of breakthrough cancer pain in Korean patients with various cancers in real-world clinical settings and supplement and expand the previous cross-sectional survey results.

NCT ID: NCT03669263 Completed - Clinical trials for Breakthrough Cancer Pain

A Dose Titration Study of Fentanyl Buccal Soluble Film for Breakthrough Cancer Pain in Taiwan

Start date: November 25, 2014
Phase: N/A
Study type: Interventional

Primary Objective: To determine the feasible dose range of Painkyl® required for Taiwanese population. Secondary Objectives: To evaluate the efficacy of Painkyl® by calculating squared mean of pain intensity difference at 30 minutes after taking Painkyl® (SPID30, an 11-point scale). To evaluate subjects' satisfaction by conducting global evaluation of medication performance (a 5-point categorical scale). To identify percentage of episodes requiring rescue medication during maintenance treatment period. To evaluate the safety data of Painkyl® for breakthrough pain.

NCT ID: NCT02899884 Completed - Clinical trials for Breakthrough Cancer Pain

Characterisation and Epidemiology of Breakthrough Cancer Pain in Spain

Start date: November 14, 2016
Phase:
Study type: Observational

The purpose of this study is to determine the prevalence of breakthrough cancer pain and characterize breakthrough cancer pain in an unselected, representative cohort of cancer outpatients with or without pain who attend consultations.

NCT ID: NCT01946555 Completed - Neuropathic Pain Clinical Trials

Prospective Longitudinal Observational Study to Evaluate the Clinical Characteristics and Opioids Treatments in Patients With Breakthrough Cancer Pain

RER
Start date: September 2013
Phase: N/A
Study type: Observational

The BTP (Breakthrough pain)was defined as "a transient exacerbation of pain that occurs either spontaneously, or in relation to a specific predictable or unpredictable trigger, despite relatively stable and adequately controlled background pain". The BTP is a common clinical features in patients with cancer pain (BTcP: breakthrough cancer pain). The prevalence of BTcP is equal to 56%. Currently, the investigators tend to recognize the idiopathic/spontaneous or accident BTcP in the three sub-types: voluntary, non- voluntary and procedural. The diagnosis of BTCP is not always easy because in the cancer patient is normal to observe changes in the intensity of pain during the day, so it is necessary to differentiate slight fluctuations from the presence of real episodes of BTCP, for which is necessary to use a rescue treatment adjusted. In the study will be proposed the use of a diagnostic algorithm, present in the literature, to perform the diagnosis of BTCP. In the presence of BTCP, is important both a correct controlled background pain with major opioids, which can reduce the number and the intensity of the painful episodes, both implement an adjunctive therapy, called "rescue", to be administered at the time which takes over the painful episode using, in this case, an opioid greater.

NCT ID: NCT01936636 Completed - Quality of Life Clinical Trials

Observational Registry Study of Quality of Life When Treating BTcP With Abstral

RELIEF
Start date: October 2013
Phase: N/A
Study type: Observational [Patient Registry]

This Observational Registry study is designed to collect self-reported Transmucosal Immediate Release Fentanyl (TIRF) Risk Evaluation and Mitigation Strategy (REMS) Access program-enrolled patient experience with breakthrough cancer pain (BTcP) as a result of treatment with Abstral® through the use of Quality of Life and pain measurement tools administered via questionnaire.

NCT ID: NCT01045603 Completed - Clinical trials for Breakthrough Cancer Pain

Instanyl® Non-Interventional Study

INIS
Start date: December 2009
Phase: N/A
Study type: Observational

The aim of this study is to describe the use of Instanyl® (Intranasal fentanyl spray) in the treatment of breakthrough pain (BTP) in cancer patients by success of dose titration and distribution of dose strength. Data will be collected at three different time points over a 3 month period.