Clinical trials: Peer Review
Peer Review, Research
Fentanyl Patch Pharmacokinetics in Healthy Adults
The study to be performed will utilize already FDA-approved marketed products in healthy adults for the purpose to generate data for establishing rate of drug delivery comparisons between RLD (reference listed drug) Duragesic ®…
- Trial name
- NCT02531971
- Testing
- Intravenous fentanyl citrate, Duragesic®, Mylan generic fentanyl
- Where
- United States
- Volunteers
- 24 people, healthy volunteers welcome
- Sponsor
- University of Maryland, Baltimore
Cancer, Prostate Cancer
Artificial Intelligence (AI)-Enhanced Pretreatment Peer-review Process to Improve Patient Safety in Radiation Oncology
This prospective study will test artificial intelligence (AI) and machine learning (ML) decision support tools. This tool is designed to help doctors, physicists and other staff during pre-treatment peer review, a step where…
- Trial name
- NCT07463833
- Testing
- The Artificial Intelligence (AI)/ Machine Learning (ML) contribution to treatment planning
- Where
- United States
- Volunteers
- 207 people, healthy volunteers welcome
- Sponsor
- UNC Lineberger Comprehensive Cancer Center
Healthy
Micropore Closure Kinetics at Various Body Sites
The study to be performed will define the rate of skin barrier recovery following micropatch application to the skin on the upper arm, volar forearm, and abdomen in healthy subjects.
- Trial name
- NCT03657277
- Testing
- Micropatch
- Where
- United States
- Volunteers
- 46 people, healthy volunteers welcome
- Sponsor
- University of Iowa
Professional Role, Research Peer Review
Delphi Process to Achieve Global Consensus on Gender Equity in Critical Care
Gender inequalities in healthcare, including among critical care professionals, have been widely recognized over the last decade.
- Trial name
- NCT06847802
- Testing
- Survey
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- Tata Memorial Centre
Peer Review, Research
Effect of Maternal and Neonatal Oxygenation
Intraoperative supplemental oxygen has been given for most parturients undergoing cesarean section under spinal anesthesia. However, evidences supporting the practice is not clear nowadays, especially for healthy parturients who…
- Trial name
- NCT01530971
- Testing
- Supplemental 3LPM oxygen via canula
- Where
- Thailand
- Volunteers
- 325 people, healthy volunteers welcome
- Sponsor
- Mahidol University
Peer Review, Research
Transdermal Patch CVD 2000: The Effect of Heat on Fentanyl Release From Fentanyl TDSs in Healthy Adults
This is an Open-label, Non-Randomized, 3-way Crossover Bioequivalence Study to compare fentanyl release after heating of a brand name (Duragesic) and generic (Apotex and Mylan) fentanyl (transdermal delivery system)TDSs in…
- Trial name
- NCT02486016
- Testing
- Duragesic reference fentanyl TDS, Apotex generic fentanyl TDS, Mylan generic fentanyl TDS
- Where
- United States
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- University of Maryland, Baltimore
Peer Review
Testing for the Presence of Authorship Bias in Peer Review
No consensus exists among biomedical journals on the subject of blinding during the peer review process. Some journals attempt to remove all identifiers of authorship from potential manuscripts before delivering to referees for…
- Trial name
- NCT02739737
- Testing
- Blinded manuscript, Unblinded manuscript
- Volunteers
- 119 people, healthy volunteers welcome
- Sponsor
- University of Washington
Peer Review, Publishing, Completeness of Reporting
Evaluating the Impact of Assessing During Peer Review the CONSORT Checklist Submitted by Authors
Randomised trials are considered the gold standard in medical research. The CONSORT (Consolidated Standards of Reporting Trials) Statement aims to improve the quality of reporting of randomised trials.
- Trial name
- NCT03751878
- Testing
- Evaluation of reporting inconsistencies, Standard Peer Review.
- Where
- United Kingdom
- Volunteers
- 24 people, healthy volunteers welcome
- Sponsor
- Universitat Politècnica de Catalunya
Healthy
Racial/Ethnic Differences in Microneedle Response
The study to be performed will define the rate of skin barrier recovery following microneedle treatment of the skin in healthy subjects of differing racial/ethnic backgrounds.
- Trial name
- NCT03332628
- Testing
- Microneedle patch
- Where
- United States
- Volunteers
- 132 people, healthy volunteers welcome
- Sponsor
- University of Iowa
Peer Review, Research
Community Members as Reviewers of Medical Journal Manuscripts
Manuscripts submitted to medical journals are typically reviewed by physicians or researchers, with no input from patients or other community members.
- Trial name
- NCT03432143
- Testing
- Community Reviewers
- Where
- United States
- Volunteers
- 568 people, healthy volunteers welcome
- Sponsor
- MetroHealth Medical Center
Peer Review
Web-based Tool to Improve the Assessment of Reporting (COBPeer)
The peer review process is a cornerstone of biomedical research publication. Despite being essential, the assessment of the completeness of the reporting and the identification of switched outcomes are not appropriately…
- Trial name
- NCT03119376
- Testing
- COBPEER
- Where
- France
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Healthy
Pharmacokinetics of Lidocaine in Healthy Adults
The study to be performed will utilize already FDA-approved marketed products in healthy adults for the purpose to generate data for establishing rate of drug delivery of Lidoderm® topical patch (manufactured by Endo…
- Trial name
- NCT03310970
- Testing
- Lidocaine 5% patch, Lidocaine hydrochloride, Lidoderm 5% patch
- Where
- United States
- Volunteers
- 23 people, healthy volunteers welcome
- Sponsor
- Nicole K Brogden
Healthy
Scopolamine Patch Pharmacokinetics in Healthy Adults
The study to be performed will utilize already FDA-approved marketed products in healthy adults for the purpose to generate data for establishing rate of drug delivery of Transderm Scop® TDDS (transdermal drug delivery system) in…
- Trial name
- NCT03029650
- Testing
- Transderm Scop®, Intravenous scopolamine hydrobromide
- Where
- United States
- Volunteers
- 26 people, healthy volunteers welcome
- Sponsor
- University of Iowa