Its precise location will be written down in the Investigator Site File. The patient data will be recorded in a case record form in CASTOR. Plans for collection, laboratory evaluation, and storage of biological specimens for genetic or molecular analysis in this trial/future use {33} Not ...
The study was approved by the Institutional Review Board of Affiliated Hospital of North Sichuan Medical College (IRB No. 2022ER146-1) and registered at chictr.org.cn (ID: ChiCTR2200058803). The subjects signed and gave the written informed consent. Using the Seldinger technique, the right ...
All patients enrolled in the study provided written informed consent, and the study was conducted in accordance with applicable International Conference on Harmonisation Good Clinical Practice Guidelines, the principles of the Declaration of Helsinki and any applicable local laws and regulations. The protoc...
After collecting written informed consent, the 111 participants will be randomly divided into three groups, with 37 participants in each group. Blinding Considering the significant contrast in content between the treatment and control groups and the lack of an impact on the therapy's final effects,...
Those who wish to take part in the trial will be asked to sign and date the written consent form, supported by the research nurse over the telephone, and return it along with their completed baseline questionnaire to the nurse in a pre-paid envelope. Those who do not wish to take part ...
The study was conducted in accordance with the principles of the Declaration of Helsinki and International Conference on Harmonisation Good Clinical Practice guidelines. All patients provided written informed consent before enrollment. The Study Protocol and Statistical Analysis Plan are available as part ...
Exclusion criteria are: age <18 years or >65 years; permanent exclusion from the workforce; inability to understand the Danish language; any serious medical condition; and lack of written informed consent. We plan to randomise 742 participants. Interventions: The experimental intervention is an ...
was registered on the Australian New Zealand Clinical Trials Registry (https://www.anzctr.org.au/—Trial Id: ACTRN12619001519145) on November 4, 2019. Each respondent gave written informed consent. All investigations were conducted according to the principles expressed in the Declaration of Helsinki...
2020, by means of posters, emails, flyers, social media, and website advertisements. Ninety participants who were in the habit of eating over more than 8 h per day and who did not have recent experience of fasting were recruited into the trial after providing their written informed consent...
This is version 2.2 of the protocol, written on January 20, 2022. The recruitment started in January 26 2022, directly after approval of the Ethics Committee. The approximate date when recruitment will be completed is estimated at the end of 2024. ...