- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01635478
A Observational Study of Assessment and Treatment Adequacy of Emergency Cancer Pain in Tertiary Cancer Hospital
July 4, 2012 updated by: DR. SWAPNIL YESHWANT PARAB, Tata Memorial Hospital
A Prospective Observational Study of Assessment of Emergency Cancer Pain and Its Treatment Adequacy in Emergency Department of Tertiary Care Cancer Hospital.
EMERGENCY CANCER PAIN MANAGEMENT HAS BEEN INCONSISTENT AND INADEQUATE ACROSS THE GLOBE.
THIS STUDY AIMS TO KNOW EMERGENCY ROOM CANCER PAIN PATTERNS AND TREATMENT ADEQUACY IN TERTIARY CARE CANCER HOSPITALS.
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Actual)
100
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
ADULT CANCER PATIENTS REPORTING TO EMERGENCY ROOM WITH COMPLAINTS PRIMARILY OF PAIN.
Description
Inclusion Criteria:
- ADULT CANCER PATIENTS REPORTING TO EMERGENCY ROOM WITH COMPLAINTS PRIMARILY OF PAIN
Exclusion Criteria:
- PATIENTS BELOW 18 YEARS OF AGE AND PATIENTS WITH INCOHERENT BEHAVIOUR.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2011
Primary Completion (Actual)
June 1, 2011
Study Completion (Actual)
June 1, 2011
Study Registration Dates
First Submitted
July 4, 2012
First Submitted That Met QC Criteria
July 4, 2012
First Posted (Estimate)
July 9, 2012
Study Record Updates
Last Update Posted (Estimate)
July 9, 2012
Last Update Submitted That Met QC Criteria
July 4, 2012
Last Verified
July 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- emcap2011
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on TO STUDY EMERGENCY CANCER PAIN PATTERNS AND TREATMENT ADEQUACY.
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Centre Hospitalier de MartiguesCompletedThis Study is to Evaluate the Prevalence | Patients Consulting the Emergency Department for Reasons Relating to General MedicineFrance
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Novartis PharmaceuticalsActive, not recruitingContinued Access to Study Treatment(s), Cancers With a Mass, Bulky Tumor, Nodule, Lump, Advanced Cancer, Advanced Solid Tumors, Advanced Solid MalignanciesUnited States, Spain, Taiwan, Singapore, France, Germany
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Dana-Farber Cancer InstituteNational Palliative Care Research CenterCompletedAdvanced Cancer | Palliative Care | Active Cancer | Active Cancer Treatment | Chronic Pain Due to CancerUnited States
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University of MonastirCompletedAge ≥18 Years | Presigned Consentement to Participate in the StudyTunisia
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University of California, IrvineRecruitingPain | Cancer | Stress | Immunotherapy | Fatigue Related to Cancer TreatmentUnited States
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Rajavithi HospitalUnknownTo Study Immunostatus of HIV-cancer Patients Who Recived RT Befor RT and Last Week of RT | To Study HIV Viral Load of HIV-cancer Patients Who Recived RT Befor RT and Last Week of RTThailand
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Umm Al-Qura UniversityCompletedSymptomatic Irreversible Pulpitis | Postoperative Endodontic Pain Following Emergency Root Canal TreatmentSaudi Arabia
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Academisch Medisch Centrum - Universiteit van Amsterdam...Ambulance Amsterdam; Stichting ZiektekostenVerzekering KrijgsmachtRecruitingAnalgesia | Emergency Medical Services | Acute Pain Due to Trauma | Fentanyl | EsketamineNetherlands
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University Hospital, Clermont-FerrandGroupama foundation; Biochemistry Lab University Hospital Clermont-FerrandRecruitingWomen and Men Over 18 Years Old | AF Ablation (ECS recommendation2020&ACS2014) Either for Paroxysmal AF Unresponsive to Anti-arrhythmic Treatment Either for Persisting Symptomatic AF | Able to Give His Non Opposition to Participate to the StudyFrance
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Michigan State UniversityCompletedFocus of Study is to Determine Efficacy of CompexUnited States