i am located in new york city and interested in setting up an idtf. i would like to get your help in that.
+11 Other Responses
I need to validate the attached result of creatinine poct to central lab results statistically with a short scientific report about the result
i am very tight in time
please let me know if you're interested asap
thank you+6 Other Responses
Medical Device Reimbursement
I want to understand how the physician and hospital payment for intracranial hemorrhage treatment for a device used in the angiography suite be different from another device used in the or setting. The scope would include identifying cpt, icd-10 and drg codes for the device used in the angio-suit; codes for the or device are already identified. +23 Other Responses
Is acetone safe for extraction of essential oils? What solvent would best extract the cannanboids from cannabus? Studies have shown compounds in cannabus kills cancer cells.
I am battleing 4th stage lymphoma and need answers fast.
erik m. Lapointe+2 Other Responses
Poct Createnin Monitoring
This project is about diabetes mellites and chronic kidney disease; poct createnin monitory
i will first give a brief about the project then describe what i need.
In this project we are analysing creatine from 20 diabetic patients by a new techniques called point of care technique poct ,which i will attach an article, as well as analysing the creatine the regular way in central lab from plasma and serum each of which were performed in duplicate.
Controls were commercially ordered.
The aim of the study is to validate these poct creatine method to the standard of the central lab and prove that there is no statistical significant different between poct and central lab result.
So in the attached excel sheet; you will have the poct in replicate from capillary and plasma in the column b,c,d,e whereas the regular cenrtal lab results in f &g
1. So the first thing we need to calculate the mean for all b,c,d,e,f,g
2. Then by using paired "t" student test from excel calculate b vs c
==>and compair between all ctrl if there is a statistically significant difference in sample
==>and if between all sample 1-20
3. Do the same thing for d vs e also if between ctr and sample 1-20
4. Do the same between f & g also if between ctr and sample 1-20
5. By using unpaired t student test analyse if b vs d vs f vs g is different?
6. Correlation "r" between b vs d vs f vs g
all these in excel as will writing a scientific description report about it
please dont hesitate to contact for any clarification in data and for any further description.
Thank you+8 Other Responses
Clinical Laboratory- Cytology
We are interested in speaking with a cytology lab expert. this question pertains to germany, france, italy, spain, brazil, mexico, china, japan, the uk, and australia.
what is the limiting factor in increasing the volume of pap testing in various markets?
what prevents 100% coverage of routine pap testing, and what prevents cytology labs from processing all samples which are currently available?
what are the major business or clinical risks facing cytology labs?+4 Other Responses
Oncologists in the eu (uk, it, ger, fr) only.
We researching to better understand clinical and prognostic practices in metastatic cancer.
As part of our research, we are hoping to gain the input of oncs in this area, and we would like to invite you to participate in a 45 minute telephone discussion with a focus on your perceptions of the clinical utility of molecular diagnostics, including circulating tumor cell (ctc) technology, in diagnosis and treatment of cancer.
Wer are offering an honorarium payment for your time and insights.
To help us see if you fit our criteria, please answer the following questions:
• how many metastatic cancer patients do you treat per month in each of the following categories?
• non-small cell lung
• diffuse large b cell lymphoma /
• follicular lymphoma
• are you a board certified oncologist?
• could you please describe your practice setting (ie, solo or group and how many physicians in our group?
We would like to schedule the interview at your earliest convenience. We are conducting these discussions from now throughout april 27th, between the hours of 8 am – 7 pm edt; that's after 2pm for most eu countries.
Thank you and we look forward to hearing from you soon!+4 Other Responses