Trial · NCT01354405
Somatostatin Analogues as a Volume Reducing Treatment of Polycystic Livers (RESOLVE)
NCT01354405, Completed, Radboud University Medical Center
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Somatostatin Analogues as a Volume Reducing Treatment of Polycystic Livers (RESOLVE). Trials, record NCT01354405. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01354405
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Somatostatin Analogues as a Volume Reducing Treatment of Polycystic Livers (RESOLVE)
- NCT number
- NCT01354405
- Status
- Completed
- Enrollment
- 43 participants, actual
- Lead sponsor
- Radboud University Medical Center
- Conditions
- Polycystic Liver Disease
- Interventions
- Lanreotide
- First posted
- 2011-05-16
- Last updated
- 2014-07-09
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Liver volume | 24 weeks | Change in total liver volume between baseline and 24 weeks, as determined by CT volumetry |
| Secondary | Kidney volume | 24 weeks | Change in kidney volume between baseline and 24 weeks, as determined by CT volumetry |
| Secondary | Glomerular filtration rate | 24 weeks | Change in GFR between baseline and 24 weeks, as determined by serum and 24 hrs urinary creatinine measurement |
| Secondary | Urinary tubular damage markers | 24 weeks | Change in urinary tubular damage markers between baseline and 24 weeks |
| Secondary | Symptoms | 24 weeks | Change in symptoms between baseline and 24 weeks, assessed by GI-questionnaire |
| Secondary | Blood pressure | 24 weeks | Change in blood pressure between baseline and 24 weeks |
| Secondary | quality of life | 24 weeks | Change in quality of life between baseline and 24 weeks, measured by EuroQoL-questionnaire |
| Secondary | Adverse events | 24 weeks | All adverse events that occur during 24 weeks of treatment |
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.
Papers3
The papers the trial lists on ClinicalTrials.gov.
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/NCT01354405
GET https://conductscience.org/api/trials/v1/NCT01354405/registered