ClinicalTrials.gov Results Submission
Budget: $250 – $750 USD
I’m ready to post the final results of our registered randomized controlled trial—a behavioral-health intervention with no drug or device component—to ClinicalTrials.gov. All participant-level data are cleaned, locked, and the main analyses are complete; what I need now is an expert who can translate those findings into a fully compliant PRS submission and shepherd it through to acceptance.
Scope of work
• Map our existing tables, figures, and outcome measures into the ClinicalTrials.gov results template, including participant flow, baseline characteristics, outcome measures, adverse events, and protocol deviations.
• Complete any additional tables/figures needed. Statistician is available to complete any additional analyses needed.
• Draft or refine the required XML fields, upload through the PRS interface, and address any automated validation errors.
• Respond promptly to reviewer comments from the ClinicalTrials.gov team until the record is publicly posted without issues.
• Provide a brief handover guide so my team can replicate the process for future trials.
Key details
– Trial type: Final results for an NIH funded RCT of a behavioral-health intervention (non-drug, non-device).
– Data status: Fully ready; Main analyses completed.
– Preferred timeline: initial draft within one week, final acceptance as quickly as the PRS review cycle allows.
- Prior experience with results reporting on ClinicalTrials.gov is required
If you have prior experience getting results records accepted on the first or second submission and are comfortable with the PRS XML schema, I’d love to work with you.
Scope of work
• Map our existing tables, figures, and outcome measures into the ClinicalTrials.gov results template, including participant flow, baseline characteristics, outcome measures, adverse events, and protocol deviations.
• Complete any additional tables/figures needed. Statistician is available to complete any additional analyses needed.
• Draft or refine the required XML fields, upload through the PRS interface, and address any automated validation errors.
• Respond promptly to reviewer comments from the ClinicalTrials.gov team until the record is publicly posted without issues.
• Provide a brief handover guide so my team can replicate the process for future trials.
Key details
– Trial type: Final results for an NIH funded RCT of a behavioral-health intervention (non-drug, non-device).
– Data status: Fully ready; Main analyses completed.
– Preferred timeline: initial draft within one week, final acceptance as quickly as the PRS review cycle allows.
- Prior experience with results reporting on ClinicalTrials.gov is required
If you have prior experience getting results records accepted on the first or second submission and are comfortable with the PRS XML schema, I’d love to work with you.