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N/A Completed N=129 Randomized Single-blind Other

Contacting Authors to Retrieve Individual Patient Data

Response Rates
Source: ClinicalTrials.gov NCT02569411 ↗
Enrolled (actual)
129
Serious AEs
Results posted
Jul 2020
Primary outcomePrimary: Proportion of Authors Who Provided Complete IPD — 0; 0 Participants

Summary

The objective of this study is to examine the impact of incentivizing authors of RCTs that are eligible for a systematic review and meta-analysis, versus usual contact strategies to obtain original IPD

Outcome Measures

OutcomeResultp-value
PRIMARY
Proportion of Authors Who Provided Complete IPD
0; 0
SECONDARY
Time Taken to Obtain the IPD Between Initial Request and Authors' Provision
SECONDARY
The Completeness of the IPD Received

Eligibility Criteria

Inclusion Criteria

  • Corresponding authors of RCTs included in our previous and updated systematic reviews

Exclusion Criteria

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02569411). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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