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Comparison · NCT00813813-ea094751

Intradiscal rhGDF-5 (0.25mg) vs Intradiscal rhGDF-5 (1.0mg): Treatment Emergent Adverse Events- Relationship to Study Drug

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Intradiscal rhGDF-5 (0.25mg) vs Intradiscal rhGDF-5 (1.0mg): Treatment Emergent Adverse Events- Relationship to Study Drug. Trial comparisons, record NCT00813813-ea094751. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00813813-ea094751

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.2860.08220.641wilson
Risk in group 20.040.00710.195wilson
Risk difference, group 1 minus group 20.246-0.01040.603newcombe hybrid score
Risk ratio, group 1 over group 27.140.75367.7log
Odds ratio, group 1 over group 29.60.723128log
Number needed to treat, for one more participant with the outcome on Intradiscal rhGDF-5 (0.25mg) than on Intradiscal rhGDF-5 (1.0mg)4.07from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Intradiscal rhGDF-5 (0.25mg)
The API is recombinant human growth and differentiation factor-5 (rhGDF-5), a recombinant version of human GDF-5. GDF-5 is a member of the transforming growth factor-b (TGF-b) superfamily and the bone morphogenetic (BMP) subfamily, and is known to influence the growth and differentiation of various tissues, including the intervertebral disc.
27OG000
Group 2Intradiscal rhGDF-5 (1.0mg)
The API is recombinant human growth and differentiation factor-5 (rhGDF-5), a recombinant version of human GDF-5. GDF-5 is a member of the transforming growth factor-b (TGF-b) superfamily and the bone morphogenetic (BMP) subfamily, and is known to influence the growth and differentiation of various tissues, including the intervertebral disc.
125OG001

Outcome

Type
PRIMARY
Title
Treatment Emergent Adverse Events- Relationship to Study Drug
Description
Number of patients with Treatment Emergent Adverse Events that were designated as related or possibly related to Study Drug.
Time frame
Through a 12 month period and annual telephone contact at 24 and 36 months for subject health status follow-up
Population
Safety Population

Source ClinicalTrials.gov

Trial

Title
Intradiscal rhGDF-5 Phase I/II Clinical Trial
NCT number
NCT00813813
Phases
PHASE1, PHASE2
Conditions
Degenerative Disc Disease
Interventions
Intradiscal rhGDF-5
Lead sponsor
DePuy Spine
Results first posted
2016-01-27

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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