Safety and Feasibility of Fasting While Receiving Chemotherapy
This study has been completed.
Sponsor:
King Fahad Medical City
Information provided by:
King Fahad Medical City
ClinicalTrials.gov Identifier:
NCT00757094
First received: September 19, 2008
Last updated: February 24, 2010
Last verified: February 2010
Tracking Information | |||||
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First Received Date ICMJE | September 19, 2008 | ||||
Last Updated Date | February 24, 2010 | ||||
Start Date ICMJE | September 2008 | ||||
Primary Completion Date | December 2008 (final data collection date for primary outcome measure) | ||||
Current Primary Outcome Measures ICMJE |
Safety of fasting while receiving chemotherapy [ Time Frame: two months ] [ Designated as safety issue: Yes ] | ||||
Original Primary Outcome Measures ICMJE | Same as current | ||||
Change History | Complete list of historical versions of study NCT00757094 on ClinicalTrials.gov Archive Site | ||||
Current Secondary Outcome Measures ICMJE |
Effect of fasting on chemotherapy side effects [ Time Frame: two months ] [ Designated as safety issue: No ] | ||||
Original Secondary Outcome Measures ICMJE | Same as current | ||||
Current Other Outcome Measures ICMJE | |||||
Original Other Outcome Measures ICMJE | |||||
Descriptive Information | |||||
Brief Title ICMJE | Safety and Feasibility of Fasting While Receiving Chemotherapy | ||||
Official Title ICMJE | Safety and Feasibility of Fasting While Receiving Chemotherapy | ||||
Brief Summary | Fasting (refraining from eating and drinking) during the day is safe while receiving chemotherapy. |
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Detailed Description | |||||
Study Type ICMJE | Observational | ||||
Study Design ICMJE | Observational Model: Case-Crossover Time Perspective: Prospective |
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Biospecimen | |||||
Sampling Method | Non-Probability Sample | ||||
Study Population | Fasting patients who are schedulled to receive chemotherapy during the month of Ramadan |
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Condition ICMJE |
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Intervention ICMJE | |||||
Study Group/Cohort (s) | I
Patients planning to observe fasting while receiving chemotherapy during the month of Ramadan |
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Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | |||||
Recruitment Status ICMJE | Completed | ||||
Enrollment ICMJE | 12 | ||||
Completion Date | March 2009 | ||||
Primary Completion Date | December 2008 (final data collection date for primary outcome measure) | ||||
Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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Gender | Both | ||||
Ages | 18 Years and older | ||||
Accepts Healthy Volunteers | No | ||||
Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
Location Countries ICMJE | Saudi Arabia | ||||
Administrative Information | |||||
NCT Number ICMJE | NCT00757094 | ||||
Other Study ID Numbers ICMJE | KFMC IRB-08-040 | ||||
Has Data Monitoring Committee | No | ||||
Responsible Party | Ali Al-Shanqeeti, King Fahad Medical City | ||||
Study Sponsor ICMJE | King Fahad Medical City | ||||
Collaborators ICMJE | |||||
Investigators ICMJE |
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Information Provided By | King Fahad Medical City | ||||
Verification Date | February 2010 | ||||
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |