Trial · NCT01621256
Efficacy, Safety, and Tolerability of Ancrod in Patients With Sudden Hearing Loss
NCT01621256, Phase 1, Phase 2, Completed, Nordmark Arzneimittel GmbH & Co. KG
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Efficacy, Safety, and Tolerability of Ancrod in Patients With Sudden Hearing Loss. Trials, record NCT01621256. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01621256
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Efficacy, Safety, and Tolerability of Ancrod in Patients With Sudden Hearing Loss
- NCT number
- NCT01621256
- Status
- Completed
- Phases
- Phase 1, Phase 2
- Enrollment
- 31 participants, actual
- Lead sponsor
- Nordmark Arzneimittel GmbH & Co. KG
- Conditions
- Hearing Loss, Deafness, Hearing Loss, Sensorineural, Hearing Disorders, Ear Diseases
- Interventions
- Ancrod, Saline solution
- First posted
- 2012-06-18
- Last updated
- 2018-12-21
- Other registries' IDs
- eudract:2012-000066-37
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in PTA (pure tone audiogram) in the affected ear | From baseline to Day 8 | |
| Secondary | Change in speech recognition in the affected ear | From baseline to Day 8 | |
| Other | Patient assessment of change in hearing impairment | From baseline to Day 8, Day 30 and Day 90 | |
| Other | Change in fibrinogen concentration | From baseline to Day 2 and Day 8 | |
| Other | Change in biomarkers | From baseline to Day 8 |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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 trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT01621256
GET https://conductscience.org/api/trials/v1/NCT01621256/registered