Comparison · NCT02495467-fb8e37b4
MED2005 vs MED Placebo: Number of Participants With Affirmative Response to Global Assessment Questionnaire (GAQ) Question 2
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. MED2005 vs MED Placebo: Number of Participants With Affirmative Response to Global Assessment Questionnaire (GAQ) Question 2. Trial comparisons, record NCT02495467-fb8e37b4. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02495467-fb8e37b4
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.394 | 0.331 | 0.46 | wilson | |
| Risk in group 2 | 0.25 | 0.197 | 0.312 | wilson | |
| Risk difference, group 1 minus group 2 | 0.144 | 0.0555 | 0.229 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.57 | 1.18 | 2.09 | log | |
| Odds ratio, group 1 over group 2 | 1.95 | 1.29 | 2.94 | log | |
| Number needed to treat, for one more participant with the outcome on MED2005 than on MED Placebo | 6.97 | 4.38 | 18 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | MED2005 | Participants who received MED2005 (0.2% glyceryl trinitrate gel). At least 4 applications of MED2005 prior to intercourse in either the first or last 4 weeks of the study. | 85 | 216 | OG001 |
| Group 2 | MED Placebo | Participants who received MED Placebo. At least 4 applications of MED Placebo prior to intercourse in either the first or last 4 weeks of the study. | 54 | 216 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants With Affirmative Response to Global Assessment Questionnaire (GAQ) Question 2
- Description
- GAQ Question 2: Has the treatment improved your ability to engage in sexual activity?. Answered yes/no after each treatment period of 4 weeks (+/- 1 week).
- Time frame
- 4 Weeks
- Population
Full Analysis Set. A total of 230 subjects reported at least one intercourse attempt and had at least one IIEF assessment in a period for which at least one intercourse attempt was reported. Complete cases only.
Source ClinicalTrials.gov
Trial
- Title
- Clinical Trial of Topically-applied Glyceryl Trinitrate (GTN) for the Treatment of Erectile Dysfunction (ED)
- NCT number
- NCT02495467
- Phases
- PHASE2
- Conditions
- Erectile Dysfunction
- Interventions
- Glyceryl trinitrate, MED Placebo
- Lead sponsor
- Futura Medical Developments Ltd.
- Results first posted
- 2020-01-29
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02495467?tab=results
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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