Trial · NCT01603394
Outcomes12
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Change From Baseline in the Daily Pain Diary (Numerical Rating Scale, NRS) Mean Pain Score at the End of the Study (Week 6). | Baseline, Week 6 | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Neuropathic Pain Symptom Inventory (NPSI) at All Visits. | All visits | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Proportion of Phenotypes Within the 30% and 50% Responder Groups at Baseline and Week 6. | Baseline, Week 6 | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Patient Global Impression of Change (PGIC) at Week 6/Early Termination. | Week 6/Early Termination | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Proportions of Participants With >/=30% and >/=50% Pain Reduction Based on Daily Pain Diary at Baseline and Week 6. | Baseline, Week 6 | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Proportion of Participants Within Each Phenotype Group as Determined by Sensory Symptom Clustering Using the PainPREDICT, PainDETECT and Neuropathic Pain Symptom Inventory at Baseline and Week 6. | Baseline, Week 6 | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Patient Health Questionnaire-8 (PHQ-8) at Baseline and Week 6; Generalized Anxiety Disorder-7 (GAD-7) at Screening, Visit 2 (Week 0) and Week 6/Early Termination. | Screening, Visit 2 (Week 0) and Week 6/Early Termination | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Brief Pain Inventory (BPI sf) at Visit 2 (Week 0) and Week 6. | Visit 2 (Week 0), Week 6 | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Patient Catastrophizing Scale (PCS) at Visit 2 (Week 0) and Week 6. | Visit 2 (Week 0), Week 6 | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Pain NRS Score; 1 Week Recall Period. | 1 Week | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Short Form 12v2 Health Survey (SF 12v2) at Visit 2 (Week 0), and Week 6/Early Termination. | Visit 2 (Week 0), and Week 6/Early Termination | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. | ||
| SECONDARY | Change From Baseline to End of the Study (Week 6) in the Daily Sleep Interference Diary (NRS) Mean Pain Score. | Baseline, Week 6 | Only 9 of the 200 participants were enrolled into the trial, so we are unable to get adequate results from this study. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
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
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT01603394/outcomes