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Trial to Assess Ch elation Therapy 2 (TACT2) NCT02733185 Informed Consent Form Version Date: 05.01.2019STUDY: TACT2 PROTOCOL NO: TACT2 STERLING IRB ID: IRB_ID DATE OF IRB REVIEW: DATE REVISED: 05/07/19PARTICIPANT
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How to fill out trial to assess chelation

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How to fill out trial to assess chelation

01
Obtain informed consent from the participant.
02
Obtain baseline blood and urine samples for analysis.
03
Administer the chelating agent according to the protocol.
04
Monitor the participant for any adverse reactions during the trial.
05
Collect follow-up blood and urine samples at specified time points.
06
Analyze the samples for changes in heavy metal levels.
07
Assess the effectiveness of chelation therapy based on the results.

Who needs trial to assess chelation?

01
Individuals with heavy metal toxicity or poisoning.
02
Individuals with chronic conditions linked to heavy metal exposure.
03
Individuals seeking alternative treatments for heavy metal detoxification.
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A trial to assess chelation is a clinical study conducted to evaluate the effectiveness and safety of chelation therapy in removing heavy metals and other toxins from the body.
Clinical researchers and sponsors conducting clinical trials involving chelation therapy are required to file for a trial to assess chelation.
To fill out a trial to assess chelation, researchers need to complete the relevant forms provided by regulatory bodies, including details about the study's design, participant eligibility, and safety protocols.
The purpose of a trial to assess chelation is to determine the efficacy of chelation therapy in treating conditions related to heavy metal toxicity and to ensure its safety for patients.
Information that must be reported includes the trial protocol, participant demographics, treatment methods, outcomes, side effects, and data analysis results.
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